ICD 11 codes page 5

From WikiMD's Wellness Encyclopedia

ICD stands for International Classification of Diseases and ICD 11 is the 11th revision.

ICD 11 Code ICD 11 Description
Pregnancy, childbirth or the puerperium
- Abortive outcome of pregnancy
JA00 - - Abortion
JA00.0 - - - Spontaneous abortion
JA00.00 - - - - Spontaneous abortion, incomplete, complicated by genital tract or pelvic infection
JA00.01 - - - - Spontaneous abortion, incomplete, complicated by delayed or excessive haemorrhage
JA00.02 - - - - Spontaneous abortion, incomplete, complicated by embolism
JA00.03 - - - - Spontaneous abortion, incomplete, with other or unspecified complications
JA00.04 - - - - Spontaneous abortion, incomplete, without complication
JA00.05 - - - - Spontaneous abortion, complete or unspecified, complicated by genital tract or pelvic infection
JA00.06 - - - - Spontaneous abortion, complete or unspecified, complicated by delayed or excessive haemorrhage
JA00.07 - - - - Spontaneous abortion, complete or unspecified, complicated by embolism
JA00.08 - - - - Spontaneous abortion, complete or unspecified, with other or unspecified complications
JA00.09 - - - - Spontaneous abortion, complete or unspecified, without complication
JA00.1 - - - Induced abortion
JA00.10 - - - - Induced abortion, incomplete, complicated by genital tract or pelvic infection
JA00.11 - - - - Induced abortion, incomplete, complicated by delayed or excessive haemorrhage
JA00.12 - - - - Induced abortion, incomplete, complicated by embolism
JA00.13 - - - - Induced abortion, incomplete, with other or unspecified complications
JA00.14 - - - - Induced abortion, incomplete, without complication
JA00.15 - - - - Induced abortion, complete or unspecified, complicated by genital tract or pelvic infection
JA00.16 - - - - Induced abortion, complete or unspecified, complicated by delayed or excessive haemorrhage
JA00.17 - - - - Induced abortion, complete or unspecified, complicated by embolism
JA00.1Y - - - - Induced abortion, complete or unspecified, with other complication
JA00.1Z - - - - Induced abortion, complete or unspecified, with unspecified complication
JA00.2 - - - Unspecified abortion
JA00.20 - - - - Unspecified abortion, incomplete, complicated by genital tract or pelvic infection
JA00.21 - - - - Unspecified abortion, incomplete, complicated by delayed or excessive haemorrhage
JA00.22 - - - - Unspecified abortion, incomplete, complicated by embolism
JA00.23 - - - - Unspecified abortion, incomplete, with other or unspecified complications
JA00.24 - - - - Unspecified abortion, incomplete, without complication
JA00.25 - - - - Unspecified abortion, complete or unspecified, complicated by genital tract or pelvic infection
JA00.26 - - - - Unspecified abortion, complete or unspecified, complicated by delayed or excessive haemorrhage
JA00.27 - - - - Unspecified abortion, complete or unspecified, complicated by embolism
JA00.28 - - - - Unspecified abortion, complete or unspecified, with other or unspecified complications
JA00.29 - - - - Unspecified abortion, complete or unspecified, without complication
JA00.3 - - - Failed attempted abortion
JA00.30 - - - - Failed medical abortion, complicated by genital tract or pelvic infection
JA00.31 - - - - Failed medical abortion, complicated by delayed or excessive haemorrhage
JA00.32 - - - - Failed medical abortion, complicated by embolism
JA00.33 - - - - Failed medical abortion, with other or unspecified complications
JA00.34 - - - - Failed medical abortion, without complication
JA00.35 - - - - Other or unspecified failed attempted abortion, complicated by genital tract or pelvic infection
JA00.36 - - - - Other or unspecified failed attempted abortion, complicated by delayed or excessive haemorrhage
JA00.37 - - - - Other or unspecified failed attempted abortion, complicated by embolism
JA00.38 - - - - Other or unspecified failed attempted abortion, with other or unspecified complications
JA00.39 - - - - Other or unspecified failed attempted abortion, without complication
JA01 - - Ectopic pregnancy
JA01.0 - - - Abdominal pregnancy
JA01.1 - - - Tubal pregnancy
JA01.2 - - - Ovarian pregnancy
JA01.Y - - - Other specified ectopic pregnancy
JA01.Z - - - Ectopic pregnancy, unspecified
JA02 - - Molar pregnancy
JA02.0 - - - Complete hydatidiform mole
JA02.1 - - - Incomplete or partial hydatidiform mole
JA02.Y - - - Other specified molar pregnancy
JA02.Z - - - Molar pregnancy, unspecified
JA03 - - Missed abortion
JA04 - - Blighted ovum or nonhydatidiform mole
JA05 - - Complications following abortion, ectopic or molar pregnancy
JA05.0 - - - Genital tract or pelvic infection following abortion, ectopic or molar pregnancy
JA05.1 - - - Delayed or excessive haemorrhage following abortion, ectopic or molar pregnancy
JA05.2 - - - Embolism following abortion, ectopic or molar pregnancy
JA05.3 - - - Shock following abortion, ectopic or molar pregnancy
JA05.4 - - - Renal failure following abortion, ectopic or molar pregnancy
JA05.5 - - - Metabolic disorders following abortion, ectopic or molar pregnancy
JA05.6 - - - Damage to pelvic organs and tissues following abortion, ectopic or molar pregnancy
JA05.7 - - - Other venous complications following abortion, ectopic or molar pregnancy
JA05.Y - - - Other specified complications following abortion, ectopic or molar pregnancy
JA05.Z - - - Complications following abortion, ectopic or molar pregnancy, unspecified
JA0Z - - Abortive outcome of pregnancy, unspecified
- Oedema, proteinuria, or hypertensive disorders in pregnancy, childbirth, or the puerperium
JA20 - - Pre-existing hypertension complicating pregnancy, childbirth or the puerperium
JA20.0 - - - Pre-existing essential hypertension complicating pregnancy, childbirth or the puerperium
JA20.1 - - - Pre-existing hypertensive heart disease complicating pregnancy, childbirth or the puerperium
JA20.2 - - - Pre-existing hypertensive renal disease complicating pregnancy, childbirth or the puerperium
JA20.3 - - - Pre-existing hypertensive heart and renal disease complicating pregnancy, childbirth or the puerperium
JA20.4 - - - Pre-existing secondary hypertension complicating pregnancy, childbirth or the puerperium
JA20.Y - - - Other specified pre-existing hypertension complicating pregnancy, childbirth or the puerperium
JA20.Z - - - Pre-existing hypertension complicating pregnancy, childbirth or the puerperium, unspecified
JA21 - - Pre-eclampsia superimposed on chronic hypertension
JA22 - - Gestational oedema or proteinuria without hypertension
JA22.0 - - - Gestational proteinuria without hypertension
JA22.1 - - - Gestational oedema without hypertension
JA22.2 - - - Gestational oedema with proteinuria, without hypertension
JA23 - - Gestational hypertension
JA24 - - Pre-eclampsia
JA24.0 - - - Mild to moderate pre-eclampsia
JA24.1 - - - Severe pre-eclampsia
JA24.2 - - - HELLP syndrome
JA24.Z - - - Pre-eclampsia, unspecified
JA25 - - Eclampsia
JA25.0 - - - Eclampsia in pregnancy
JA25.1 - - - Eclampsia in labour
JA25.2 - - - Eclampsia in the puerperium
JA25.3 - - - Eclampsia, time period unspecified
JA2Z - - Oedema, proteinuria, or hypertensive disorders in pregnancy, childbirth, or the puerperium, unspecified
- Obstetric haemorrhage
JA40 - - Haemorrhage in early pregnancy
JA40.0 - - - Threatened abortion
JA40.Y - - - Other specified haemorrhage in early pregnancy
JA41 - - Antepartum haemorrhage
JA41.0 - - - Antepartum haemorrhage with coagulation defect
JA41.Y - - - Other specified antepartum haemorrhage
JA41.Z - - - Antepartum haemorrhage, unspecified
JA42 - - Intrapartum haemorrhage
JA42.0 - - - Intrapartum haemorrhage with coagulation defect
JA42.1 - - - Intrapartum haemorrhage resulting from obstructed labour with uterine rupture
JA42.2 - - - Intrapartum haemorrhage resulting from obstructed labour without mention of uterine rupture
JA42.Y - - - Other specified intrapartum haemorrhage
JA42.Z - - - Intrapartum haemorrhage, unspecified
JA43 - - Postpartum haemorrhage
JA43.0 - - - Third-stage haemorrhage
JA43.1 - - - Other immediate postpartum haemorrhage
JA43.2 - - - Delayed or secondary postpartum haemorrhage
JA43.3 - - - Postpartum coagulation defects
JA43.4 - - - Postpartum haemorrhage following obstructed labour with uterine rupture
JA43.5 - - - Postpartum haemorrhage following obstructed labour without mention of uterine rupture
JA43.Y - - - Other specified postpartum haemorrhage
JA43.Z - - - Postpartum haemorrhage, unspecified
JA4Z - - Obstetric haemorrhage, unspecified
- Certain specified maternal disorders predominantly related to pregnancy
JA60 - - Excessive vomiting in pregnancy
JA60.0 - - - Mild hyperemesis gravidarum
JA60.1 - - - Hyperemesis gravidarum with metabolic disturbance
JA60.2 - - - Late vomiting of pregnancy
JA60.Y - - - Other specified excessive vomiting in pregnancy
JA60.Z - - - Excessive vomiting in pregnancy, unspecified
JA61 - - Venous complications in pregnancy
JA61.0 - - - Varicose veins of lower extremity in pregnancy
JA61.1 - - - Genital varices in pregnancy
JA61.2 - - - Superficial thrombophlebitis in pregnancy
JA61.3 - - - Deep phlebothrombosis in pregnancy
JA61.4 - - - Haemorrhoids in pregnancy
JA61.5 - - - Cerebral venous thrombosis in pregnancy
JA61.Y - - - Other specified venous complications in pregnancy
JA61.Z - - - Venous complications in pregnancy, unspecified
JA62 - - Infections of genitourinary tract in pregnancy
JA62.0 - - - Infections of kidney in pregnancy
JA62.1 - - - Infections of bladder in pregnancy
JA62.2 - - - Infections of urethra in pregnancy
JA62.3 - - - Infections of other parts of urinary tract in pregnancy
JA62.4 - - - Infections of the genital tract in pregnancy
JA62.Y - - - Infections of genitourinary tract in pregnancy, other specified site
JA62.Z - - - Infection of genitourinary tract in pregnancy, site unspecified
JA63 - - Diabetes mellitus in pregnancy
JA63.0 - - - Pre-existing type 1 diabetes mellitus in pregnancy
JA63.1 - - - Pre-existing type 2 diabetes mellitus in pregnancy
JA63.2 - - - Diabetes mellitus arising in pregnancy
JA63.Y - - - Other specified diabetes mellitus in pregnancy
JA63.Z - - - Diabetes mellitus in pregnancy, unspecified
JA64 - - Malnutrition in pregnancy
JA65 - - Maternal care for other conditions predominantly related to pregnancy
JA65.0 - - - Liver disorders in pregnancy, childbirth or the puerperium
JA65.1 - - - Pregnancy dermatoses
JA65.10 - - - - Gestational pemphigoid
JA65.11 - - - - Pruritus of pregnancy
JA65.12 - - - - Polymorphic eruption of pregnancy
JA65.1Y - - - - Other specified pregnancy dermatoses
JA65.2 - - - Excessive weight gain in pregnancy
JA65.3 - - - Low weight gain in pregnancy
JA65.4 - - - Pregnancy care of habitual aborter
JA65.5 - - - Retained intrauterine contraceptive device in pregnancy
JA65.6 - - - Maternal hypotension syndrome
JA65.7 - - - Subluxation of symphysis pubis in pregnancy, childbirth or the puerperium
JA65.Y - - - Maternal care for other specified conditions predominantly related to pregnancy
JA65.Z - - - Maternal care for unspecified conditions predominantly related to pregnancy
JA66 - - Clinical findings on antenatal screening of mother
JA66.0 - - - Abnormal haematological finding on antenatal screening of mother
JA66.1 - - - Abnormal biochemical finding on antenatal screening of mother
JA66.2 - - - Abnormal cytological finding on antenatal screening of mother
JA66.3 - - - Abnormal ultrasonic finding on antenatal screening of mother
JA66.4 - - - Abnormal radiological finding on antenatal screening of mother
JA66.5 - - - Abnormal chromosomal or genetic finding on antenatal screening of mother
JA66.Y - - - Other specified clinical findings on antenatal screening of mother
JA66.Z - - - Clinical findings on antenatal screening of mother, unspecified
JA67 - - Complications of anaesthesia during pregnancy
JA67.0 - - - Pulmonary complications of anaesthesia during pregnancy
JA67.1 - - - Cardiac complications of anaesthesia during pregnancy
JA67.2 - - - Central nervous system complications of anaesthesia during pregnancy
JA67.3 - - - Toxic reaction to local anaesthesia during pregnancy
JA67.4 - - - Spinal or epidural anaesthesia-induced headache during pregnancy
JA67.5 - - - Failed or difficult intubation during pregnancy
JA67.Y - - - Other specified complications of anaesthesia during pregnancy
JA67.Z - - - Complications of anaesthesia during pregnancy, unspecified
JA6Z - - Maternal disorders predominantly related to pregnancy, unspecified
- Maternal care related to the foetus, amniotic cavity or possible delivery problems
JA80 - - Maternal care related to multiple gestation
JA80.0 - - - Twin pregnancy
JA80.1 - - - Triplet pregnancy
JA80.2 - - - Quadruplet pregnancy
JA80.Y - - - Other specified maternal care related to multiple gestation
JA80.Z - - - Maternal care related to multiple gestation, unspecified
JA81 - - Maternal care related to complications specific to multiple gestation
JA81.0 - - - Papyraceous foetus
JA81.1 - - - Continuing pregnancy after abortion of one foetus or more
JA81.2 - - - Continuing pregnancy after intrauterine death of one foetus or more
JA81.3 - - - Loss of pregnancy after abortion or intrauterine death of one foetus or more
JA81.Y - - - Other specified maternal care related to complications specific to multiple gestation
JA81.Z - - - Maternal care related to complications specific to multiple gestation, unspecified
JA82 - - Maternal care for known or suspected malpresentation of foetus
JA82.0 - - - Maternal care for unstable lie
JA82.1 - - - Maternal care for breech presentation
JA82.2 - - - Maternal care for transverse or oblique lie
JA82.3 - - - Maternal care for face, brow or chin presentation
JA82.4 - - - Maternal care for high head at term
JA82.5 - - - Maternal care for multiple gestation with malpresentation of one foetus or more
JA82.6 - - - Maternal care for compound presentation
JA82.Y - - - Maternal care for known or suspected other specified malpresentation of fetus
JA82.Z - - - Maternal care for known or suspected malpresentation of foetus, unspecified
JA83 - - Maternal care for known or suspected disproportion
JA83.0 - - - Maternal care for disproportion due to deformity of maternal pelvic bones
JA83.1 - - - Maternal care for disproportion due to generally contracted pelvis
JA83.2 - - - Maternal care for disproportion due to inlet contraction of pelvis
JA83.3 - - - Maternal care for disproportion due to outlet contraction of pelvis
JA83.4 - - - Maternal care for disproportion of mixed maternal and foetal origin
JA83.5 - - - Maternal care for disproportion due to unusually large foetus
JA83.6 - - - Maternal care for disproportion due to hydrocephalic foetus
JA83.Y - - - Maternal care for known or suspected other specified disproportion
JA83.Z - - - Maternal care for known or suspected disproportion, unspecified
JA84 - - Maternal care for known or suspected abnormality of pelvic organs
JA84.0 - - - Maternal care for congenital malformation of uterus
JA84.1 - - - Maternal care for tumour of corpus uteri
JA84.2 - - - Maternal care due to uterine scar from previous surgery
JA84.3 - - - Maternal care for cervical incompetence
JA84.4 - - - Maternal care for abnormality of vagina
JA84.5 - - - Maternal care for abnormality of vulva or perineum
JA84.Y - - - Maternal care for known or suspected other specified abnormality of pelvic organs
JA84.Z - - - Maternal care for known or suspected abnormality of pelvic organs, unspecified
JA85 - - Maternal care for known or suspected foetal abnormality or damage
JA85.0 - - - Maternal care for known or suspected central nervous system malformation in foetus
JA85.1 - - - Maternal care for known or suspected chromosomal abnormality in foetus
JA85.2 - - - Maternal care for known or suspected hereditary disease in foetus
JA85.3 - - - Maternal care for known or suspected damage to foetus from viral disease in mother
JA85.Y - - - Maternal care for known or suspected other specified fetal abnormality or damage
JA85.Z - - - Maternal care for known or suspected foetal abnormality or damage, unspecified
JA86 - - Maternal care for other known or suspected foetal problems
JA86.0 - - - Maternal care for red cell antibodies
JA86.1 - - - Maternal care for hydrops fetalis
JA86.2 - - - Maternal care for signs of foetal hypoxia
JA86.3 - - - Maternal care for intrauterine death
JA86.4 - - - Maternal care for foetal growth restriction
JA86.5 - - - Maternal care for suspected macrosomia
JA86.6 - - - Maternal care for viable foetus in abdominal pregnancy
JA86.Y - - - Maternal care for other specified fetal problems
JA86.Z - - - Maternal care for other known or suspected foetal problems, unspecified
JA87 - - Maternal care related to polyhydramnios
JA88 - - Maternal care related to certain specified disorders of amniotic fluid or membranes
JA88.0 - - - Oligohydramnios
JA88.1 - - - Infection of amniotic sac or membranes
JA88.Y - - - Other specified disorders of amniotic fluid and membranes
JA88.Z - - - Disorders of amniotic fluid and membranes, unspecified
JA89 - - Maternal care related to premature rupture of membranes
JA89.0 - - - Premature rupture of membranes, onset of labour within 24 hours
JA89.1 - - - Premature rupture of membranes, onset of labour after 24 hours
JA89.2 - - - Premature rupture of membranes, labour delayed by therapy
JA89.3 - - - Preterm premature rupture of membranes
JA89.Y - - - Other specified maternal care related to premature rupture of membranes
JA89.Z - - - Maternal care related to premature rupture of membranes, unspecified
JA8A - - Maternal care related to placental disorders
JA8A.0 - - - Placental transfusion syndromes
JA8A.1 - - - Malformation of placenta
JA8A.2 - - - Morbidly adherent placenta
JA8A.Y - - - Other specified maternal care related to placental disorders
JA8A.Z - - - Maternal care related to placental disorders, unspecified
JA8B - - Maternal care related to placenta praevia or low lying placenta
JA8B.0 - - - Placenta praevia specified as without haemorrhage
JA8B.1 - - - Placenta praevia with haemorrhage
JA8B.Z - - - Maternal care related to placenta praevia or low lying placenta, unspecified
JA8C - - Maternal care related to premature separation of placenta
JA8C.0 - - - Premature separation of placenta with coagulation defect
JA8C.Y - - - Other specified maternal care related to premature separation of placenta
JA8C.Z - - - Maternal care related to premature separation of placenta, unspecified
JA8D - - Maternal care related to false labour
JA8D.0 - - - False labour before 37 completed weeks of gestation
JA8D.1 - - - False labour at or after 37 completed weeks of gestation
JA8D.Z - - - Maternal care related to false labour, unspecified
JA8E - - Maternal care related to prolonged pregnancy
JA8Y - - Maternal care related to other specified fetus, amniotic cavity or possible delivery problems
JA8Z - - Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems
- Complications of labour or delivery
JB00 - - Preterm labour or delivery
JB00.0 - - - Preterm labour without delivery
JB00.1 - - - Preterm spontaneous labour with preterm delivery
JB00.2 - - - Preterm labour with term delivery
JB00.3 - - - Preterm delivery following iatrogenic induction of labour or caesarean section
JB00.Y - - - Other specified preterm labour or delivery
JB00.Z - - - Preterm labour or delivery, unspecified
JB01 - - Failed induction of labour
JB01.0 - - - Failed medical induction of labour
JB01.1 - - - Failed instrumental induction of labour
JB01.Z - - - Failed induction of labour, unspecified
JB02 - - Abnormalities of forces of labour
JB02.0 - - - Primary uterine inertia
JB02.1 - - - Secondary uterine inertia
JB02.2 - - - Other uterine inertia
JB02.3 - - - Precipitate labour
JB02.4 - - - Hypertonic, incoordinate, or prolonged uterine contractions
JB02.Y - - - Other specified abnormalities of forces of labour
JB02.Z - - - Abnormalities of forces of labour, unspecified
JB03 - - Long labour
JB03.0 - - - Prolonged first stage of labour
JB03.1 - - - Prolonged second stage of labour
JB03.2 - - - Delayed delivery of successive neonates
JB03.Z - - - Long labour, unspecified
JB04 - - Obstructed labour due to malposition or malpresentation of foetus
JB04.0 - - - Obstructed labour due to incomplete rotation of foetal head
JB04.1 - - - Obstructed labour due to breech presentation
JB04.2 - - - Obstructed labour due to face presentation
JB04.3 - - - Obstructed labour due to brow presentation
JB04.4 - - - Obstructed labour due to shoulder presentation
JB04.5 - - - Obstructed labour due to compound presentation
JB04.Y - - - Obstructed labour due to other malposition and malpresentation of fetus
JB04.Z - - - Obstructed labour due to malposition or malpresentation of foetus, unspecified
JB05 - - Obstructed labour due to maternal pelvic abnormality
JB05.0 - - - Obstructed labour due to deformed pelvis
JB05.1 - - - Obstructed labour due to generally contracted pelvis
JB05.2 - - - Obstructed labour due to pelvic inlet contraction
JB05.3 - - - Obstructed labour due to pelvic outlet or mid-cavity contraction
JB05.4 - - - Obstructed labour due to foetopelvic disproportion, unspecified
JB05.5 - - - Obstructed labour due to abnormality of maternal pelvic organs
JB05.Y - - - Obstructed labour due to other maternal pelvic abnormalities
JB05.Z - - - Obstructed labour due to maternal pelvic abnormality, unspecified
JB06 - - Obstructed labour due to other causes
JB06.0 - - - Obstructed labour due to shoulder dystocia
JB06.1 - - - Obstructed labour due to locked twins
JB06.2 - - - Obstructed labour due to unusually large foetus
JB06.3 - - - Obstructed labour due to other abnormalities of foetus
JB06.Y - - - Obstructed labour due to other specified causes
JB06.Z - - - Obstructed labour due to unspecified causes
JB07 - - Labour or delivery complicated by foetal distress
JB07.0 - - - Labour or delivery complicated by foetal heart rate anomaly
JB07.1 - - - Labour or delivery complicated by meconium in amniotic fluid
JB07.2 - - - Labour or delivery complicated by biochemical evidence of foetal stress
JB07.Y - - - Other specified labour or delivery complicated by foetal distress
JB07.Z - - - Labour or delivery complicated by foetal distress, unspecified
JB08 - - Labour or delivery complicated by umbilical cord complications
JB08.0 - - - Labour or delivery complicated by prolapse of cord
JB08.1 - - - Labour or delivery complicated by cord around neck, with compression
JB08.2 - - - Labour or delivery complicated by short cord
JB08.3 - - - Labour or delivery complicated by vasa praevia
JB08.4 - - - Labour or delivery complicated by vascular lesion of cord
JB08.Y - - - Labour and delivery complicated by other specified umbilical cord complications
JB08.Z - - - Labour or delivery complicated by umbilical cord complications, unspecified
JB09 - - Perineal laceration during delivery
JB09.0 - - - First degree perineal laceration during delivery
JB09.1 - - - Second degree perineal laceration during delivery
JB09.2 - - - Third degree perineal laceration during delivery
JB09.3 - - - Fourth degree perineal laceration during delivery
JB09.Y - - - Other specified perineal laceration during delivery
JB09.Z - - - Perineal laceration during delivery, unspecified
JB0A - - Certain specified obstetric trauma
JB0A.0 - - - Rupture of uterus before onset of labour
JB0A.1 - - - Rupture of uterus during labour
JB0A.2 - - - Postpartum inversion of uterus
JB0A.3 - - - Obstetric laceration of cervix
JB0A.4 - - - Obstetric high vaginal laceration alone
JB0A.5 - - - Obstetric uterine laceration or tear
JB0A.6 - - - Other obstetric injury to pelvic organs
JB0A.7 - - - Obstetric damage to pelvic joints or ligaments
JB0A.8 - - - Obstetric haematoma of pelvis
JB0A.Y - - - Other specified obstetric trauma
JB0A.Z - - - Obstetric trauma, unspecified
JB0B - - Retained placenta or membranes, without haemorrhage
JB0B.0 - - - Retained placenta without haemorrhage
JB0B.1 - - - Retained portions of placenta or membranes, without haemorrhage
JB0C - - Complications of anaesthesia during labour or delivery
JB0C.0 - - - Aspiration pneumonitis due to anaesthesia during labour or delivery
JB0C.1 - - - Other pulmonary complications of anaesthesia during labour or delivery
JB0C.2 - - - Cardiac complications of anaesthesia during labour or delivery
JB0C.3 - - - Central nervous system complications of anaesthesia during labour or delivery
JB0C.4 - - - Toxic reaction to local anaesthesia during labour or delivery
JB0C.5 - - - Spinal or epidural anaesthesia-induced headache during labour or delivery
JB0C.6 - - - Other complications of spinal or epidural anaesthesia during labour or delivery
JB0C.7 - - - Failed or difficult intubation during labour or delivery
JB0C.Y - - - Other specified complications of anaesthesia during labour or delivery
JB0C.Z - - - Complications of anaesthesia during labour or delivery, unspecified
JB0D - - Certain specified complications of labour or delivery, not elsewhere classified
JB0D.0 - - - Maternal distress during labour or delivery
JB0D.1 - - - Shock during or following labour or delivery
JB0D.2 - - - Pyrexia during labour, not elsewhere classified
JB0D.3 - - - Other complications of obstetric surgery or procedures
JB0D.4 - - - Delayed delivery after artificial rupture of membranes
JB0D.5 - - - Delayed delivery after spontaneous or unspecified rupture of membranes
JB0D.6 - - - Vaginal delivery following previous caesarean section
JB0D.7 - - - Failed application of vacuum extractor or forceps, unspecified
JB0D.8 - - - Failed trial of labour, unspecified
JB0D.Y - - - Other specified complications of labour or delivery, not elsewhere classified
JB0Y - - Other specified complications of labour or delivery
JB0Z - - Complications of labour or delivery, unspecified
- Delivery
JB20 - - Single spontaneous delivery
JB20.0 - - - Spontaneous vertex delivery
JB20.1 - - - Spontaneous breech delivery
JB20.Y - - - Single spontaneous delivery with other specified presentation
JB20.Z - - - Single spontaneous delivery, unspecified
JB21 - - Single delivery by forceps or vacuum extractor
JB22 - - Single delivery by caesarean section
JB22.0 - - - Delivery by elective caesarean section
JB22.1 - - - Delivery by emergency caesarean section
JB22.2 - - - Single delivery by caesarean hysterectomy
JB22.Z - - - Single delivery by caesarean section, unspecified
JB23 - - Other assisted single delivery
JB23.0 - - - Breech extraction
JB23.1 - - - Other assisted breech delivery
JB23.2 - - - Other manipulation-assisted delivery
JB23.3 - - - Delivery of viable foetus in abdominal pregnancy
JB23.4 - - - Destructive operation for delivery
JB23.Z - - - Other assisted single delivery, unspecified
JB24 - - Multiple delivery
JB24.0 - - - Multiple delivery, all spontaneous
JB24.1 - - - Multiple delivery, all by forceps or vacuum extractor
JB24.2 - - - Multiple delivery, all by caesarean section
JB24.3 - - - Multiple delivery by combination of methods with caesarean
JB24.Y - - - Other specified multiple delivery
JB24.Z - - - Multiple delivery, unspecified
JB2Z - - Delivery, unspecified
- Complications predominantly related to the puerperium
JB40 - - Infections in the puerperium
JB40.0 - - - Puerperal sepsis
JB40.1 - - - Infection of obstetric surgical wound
JB40.2 - - - Other infection of genital tract following delivery
JB40.3 - - - Urinary tract infection following delivery
JB40.4 - - - Pyrexia of unknown origin following delivery
JB40.Y - - - Other specified infections in the puerperium
JB40.Z - - - Infections in the puerperium, unspecified
JB41 - - Venous complications in the puerperium
JB41.0 - - - Superficial thrombophlebitis in the puerperium
JB41.1 - - - Deep phlebothrombosis in the puerperium
JB41.2 - - - Haemorrhoids in the puerperium
JB41.3 - - - Cerebral venous thrombosis in the puerperium
JB41.Y - - - Other specified venous complications in the puerperium
JB41.Z - - - Venous complications in the puerperium, unspecified
JB42 - - Obstetric embolism
JB42.0 - - - Obstetric air embolism
JB42.1 - - - Amniotic fluid embolism
JB42.2 - - - Obstetric blood-clot embolism
JB42.3 - - - Obstetric pyaemic or septic embolism
JB42.Y - - - Other specified obstetric embolism
JB42.Z - - - Obstetric embolism, unspecified
JB43 - - Complications of anaesthesia during the puerperium
JB43.0 - - - Pulmonary complications of anaesthesia during the puerperium
JB43.1 - - - Cardiac complications of anaesthesia during the puerperium
JB43.2 - - - Central nervous system complications of anaesthesia during the puerperium
JB43.3 - - - Spinal or epidural anaesthesia-induced headache during the puerperium
JB43.4 - - - Other complications of spinal or epidural anaesthesia during the puerperium
JB43.5 - - - Failed or difficult intubation during the puerperium
JB43.Y - - - Other specified complications of anaesthesia during the puerperium
JB43.Z - - - Complications of anaesthesia during the puerperium, unspecified
JB44 - - Certain specified complications of the puerperium
JB44.0 - - - Disruption of caesarean section wound
JB44.1 - - - Disruption of perineal obstetric wound
JB44.2 - - - Haematoma of obstetric wound
JB44.3 - - - Cardiomyopathy in the puerperium
JB44.4 - - - Postpartum acute renal failure
JB44.5 - - - Postpartum thyroiditis
JB44.6 - - - Puerperal osteomalacia
JB44.Y - - - Other specified complications of the puerperium
JB44.Z - - - Complications of the puerperium, unspecified
JB45 - - Infections of breast associated with childbirth
JB45.0 - - - Abscess of breast associated with childbirth
JB45.1 - - - Nonpurulent mastitis associated with childbirth
JB45.Y - - - Other specified infections of breast associated with childbirth
JB45.Z - - - Infections of breast associated with childbirth, unspecified
JB46 - - Certain specified disorders of breast or lactation associated with childbirth
JB46.0 - - - Retracted nipple associated with childbirth
JB46.1 - - - Cracked nipple associated with childbirth
JB46.2 - - - Other or unspecified disorders of breast associated with childbirth
JB46.3 - - - Agalactia
JB46.4 - - - Hypogalactia
JB46.5 - - - Suppressed lactation
JB46.6 - - - Galactorrhoea
JB46.7 - - - Other or unspecified disorders of lactation
JB4Z - - Complications predominantly related to the puerperium, unspecified
- Certain obstetric conditions, not elsewhere classified
JB60 - - Obstetric death of unspecified cause
JB61 - - Death from any obstetric cause occurring more than 42 days but less than one year after delivery
JB62 - - Death from sequelae of obstetric causes
JB62.0 - - - Death from sequelae of direct obstetric cause
JB62.1 - - - Death from sequelae of indirect obstetric cause
JB62.Z - - - Death from sequelae of obstetric causes, unspecified
JB63 - - Maternal infectious diseases classifiable elsewhere but complicating pregnancy, childbirth or the puerperium
JB63.0 - - - Tuberculosis complicating pregnancy, childbirth or the puerperium
JB63.00 - - - - Tuberculous placenta
JB63.0Y - - - - Other specified tuberculosis complicating pregnancy, childbirth or the puerperium
JB63.0Z - - - - Tuberculosis complicating pregnancy, childbirth or the puerperium, unspecified
JB63.1 - - - Syphilis complicating pregnancy, childbirth or the puerperium
JB63.2 - - - Gonorrhoea complicating pregnancy, childbirth or the puerperium
JB63.3 - - - Other infections with a predominantly sexual mode of transmission complicating pregnancy, childbirth or the puerperium
JB63.4 - - - Viral hepatitis complicating pregnancy, childbirth or the puerperium
JB63.5 - - - Other viral diseases complicating pregnancy, childbirth or the puerperium
JB63.6 - - - Protozoal diseases complicating pregnancy, childbirth or the puerperium
JB63.60 - - - - Malaria complicating pregnancy, childbirth, or the puerperium
JB63.6Y - - - - Other specified protozoal diseases complicating pregnancy, childbirth or the puerperium
JB63.6Z - - - - Protozoal diseases complicating pregnancy, childbirth or the puerperium, unspecified
JB63.7 - - - Human immunodeficiency disease complicating pregnancy, childbirth or the puerperium
JB63.Y - - - Other specified maternal infectious diseases classifiable elsewhere but complicating pregnancy, childbirth or the puerperium
JB63.Z - - - Maternal infectious diseases classifiable elsewhere but complicating pregnancy, childbirth or the puerperium, unspecified
JB64 - - Certain maternal diseases classifiable elsewhere but complicating pregnancy, childbirth or the puerperium
JB64.0 - - - Anaemia complicating pregnancy, childbirth or the puerperium
JB64.1 - - - Other diseases of the blood or blood-forming organs or certain disorders involving the immune mechanism complicating pregnancy, childbirth or the puerperium
JB64.2 - - - Endocrine, nutritional or metabolic diseases complicating pregnancy, childbirth or the puerperium
JB64.3 - - - Diseases of the nervous system complicating pregnancy, childbirth or the puerperium
JB64.4 - - - Diseases of the circulatory system complicating pregnancy, childbirth or the puerperium
JB64.5 - - - Diseases of the respiratory system complicating pregnancy, childbirth or the puerperium
JB64.6 - - - Diseases of the digestive system complicating pregnancy, childbirth or the puerperium
JB64.7 - - - Diseases of the skin or subcutaneous tissue complicating pregnancy, childbirth or the puerperium
JB64.8 - - - Congenital anomaly complicating pregnancy
JB64.Y - - - Other specified maternal diseases classifiable elsewhere but complicating pregnancy, childbirth or the puerperium
JB64.Z - - - Maternal diseases classifiable elsewhere but complicating pregnancy, childbirth or the puerperium, unspecified
JB65 - - Sequelae of complication of pregnancy, childbirth or the puerperium
JB6Y - - Other specified obstetric conditions, not elsewhere classified
JB6Z - - Unspecified obstetric condition
Certain conditions originating in the perinatal period
- Foetus or newborn affected by maternal factors or by complications of pregnancy, labour or delivery
KA00 - - Foetus or newborn affected by maternal conditions that may be unrelated to present pregnancy
KA00.0 - - - Foetus or newborn affected by maternal hypertensive disorders
KA00.1 - - - Foetus or newborn affected by gestational oedema or proteinuria without hypertension
KA00.2 - - - Foetus or newborn affected by maternal renal or urinary tract diseases
KA00.3 - - - Foetus or newborn affected by maternal infectious diseases
KA00.4 - - - Foetus or newborn affected by periodontal disease in mother
KA00.5 - - - Foetus or newborn affected by maternal respiratory diseases
KA00.6 - - - Foetus or newborn affected by maternal nutritional disorders
KA00.60 - - - - Foetus or newborn affected by maternal malnutrition
KA00.61 - - - - Foetus or newborn affected by maternal overweight or obesity
KA00.6Y - - - - Other specified foetus or newborn affected by maternal nutritional disorders
KA00.6Z - - - - Foetus or newborn affected by maternal nutritional disorders, unspecified
KA00.7 - - - Foetus or newborn affected by abnormal maternal chemistry
KA00.8 - - - Foetus or newborn affected by maternal injury
KA00.9 - - - Foetus or newborn affected by maternal chemotherapy
KA00.A - - - Foetus or newborn affected by surgical procedure on mother
KA00.B - - - Foetus or newborn affected by maternal anaemia
KA00.Y - - - Other specified foetus or newborn affected by maternal conditions that may be unrelated to present pregnancy
KA00.Z - - - Foetus or newborn affected by maternal conditions that may be unrelated to present pregnancy, unspecified
KA01 - - Foetus or newborn affected by maternal complications of pregnancy
KA01.0 - - - Foetus or newborn affected by incompetence of cervix uteri
KA01.1 - - - Foetus or newborn affected by premature rupture of membranes
KA01.2 - - - Foetus or newborn affected by oligohydramnios
KA01.3 - - - Foetus or newborn affected by polyhydramnios
KA01.4 - - - Foetus or newborn affected by ectopic pregnancy
KA01.5 - - - Foetus or newborn affected by multiple pregnancy
KA01.6 - - - Foetus or newborn affected by maternal death
KA01.7 - - - Foetus or newborn affected by malpresentation before labour
KA01.8 - - - Foetus or newborn affected by maternal blood loss
KA01.Y - - - Other specified foetus or newborn affected by maternal complications of pregnancy
KA01.Z - - - Foetus or newborn affected by maternal complications of pregnancy, unspecified
KA02 - - Foetus or newborn affected by complications of placenta
KA02.0 - - - Foetus or newborn affected by placenta praevia
KA02.1 - - - Foetus or newborn affected by placental oedema or large placenta
KA02.2 - - - Foetus or newborn affected by placental infarction
KA02.3 - - - Foetus or newborn affected by placental insufficiency or small placenta
KA02.4 - - - Foetus or newborn affected by placental transfusion syndromes
KA02.Y - - - Other specified foetus or newborn affected by complications of placenta
KA02.Z - - - Foetus or newborn affected by complications of placenta, unspecified
KA03 - - Foetus or newborn affected by complications of umbilical cord
KA03.0 - - - Foetus or newborn affected by prolapsed cord
KA03.1 - - - Foetus or newborn affected by other compression of umbilical cord
KA03.2 - - - Foetus or newborn affected by abnormalities of umbilical cord length
KA03.20 - - - - Foetus or newborn affected by short umbilical cord
KA03.21 - - - - Foetus or newborn affected by long umbilical cord
KA03.2Y - - - - Other specified foetus or newborn affected by abnormalities of umbilical cord length
KA03.2Z - - - - Foetus or newborn affected by abnormalities of umbilical cord length, unspecified
KA03.3 - - - Foetus or newborn affected by vasa praevia
KA03.4 - - - Foetus or newborn affected by traumatic injury of the umbilical cord
KA03.Y - - - Other specified foetus or newborn affected by complications of umbilical cord
KA03.Z - - - Foetus or newborn affected by complications of umbilical cord, unspecified
KA04 - - Foetus or newborn affected by other abnormalities of membranes
KA04.0 - - - Foetus or newborn affected by chorioamnionitis
KA04.1 - - - Foetus or newborn affected by amniotic Band Syndrome
KA04.Y - - - Other specified foetus or newborn affected by other abnormalities of membranes
KA04.Z - - - Foetus or newborn affected by other abnormalities of membranes, unspecified
KA05 - - Foetus or newborn affected by certain complications of labour or delivery
KA05.0 - - - Foetus or newborn affected by breech delivery or extraction
KA05.1 - - - Foetus or newborn affected by other malpresentation, malposition or disproportion during labour or delivery
KA05.2 - - - Foetus or newborn affected by forceps delivery
KA05.3 - - - Foetus or newborn affected by delivery by vacuum extractor
KA05.4 - - - Foetus or newborn affected by caesarean delivery
KA05.5 - - - Foetus or newborn affected by precipitate delivery
KA05.6 - - - Foetus or newborn affected by abnormal uterine contractions
KA05.7 - - - Foetus or newborn affected by abnormality in foetal intrauterine heart rate or rhythm
KA05.70 - - - - Foetus and newborn affected by abnormality in foetal intrauterine heart rate or rhythm before onset of labour
KA05.71 - - - - Foetus and newborn affected by abnormality in foetal intrauterine heart rate or rhythm during labour
KA05.7Y - - - - Other specified foetus or newborn affected by abnormality in foetal intrauterine heart rate or rhythm
KA05.7Z - - - - Foetus or newborn affected by abnormality in foetal intrauterine heart rate or rhythm, unspecified
KA05.8 - - - Meconium passage during delivery
KA05.Y - - - Fetus or newborn affected or suspected to be affected by other specified complications of labour or delivery
KA05.Z - - - Fetus or newborn affected or suspected to be affected by unspecified complications of labour or delivery
KA06 - - Foetus or newborn affected by noxious influences transmitted via placenta or breast milk
KA06.0 - - - Foetus or newborn affected by maternal anaesthesia or analgesia in pregnancy, labour or delivery
KA06.1 - - - Foetus or newborn affected by maternal use of tobacco
KA06.2 - - - Foetus or newborn affected by maternal use of alcohol
KA06.3 - - - Foetus or newborn affected by maternal use of drugs of addiction
KA06.4 - - - Foetus or newborn affected by maternal use of nutritional chemical substances
KA06.5 - - - Foetus or newborn affected by maternal exposure to environmental chemical substances
KA06.Y - - - Other specified foetus or newborn affected by noxious influences transmitted via placenta or breast milk
KA06.Z - - - Foetus or newborn affected by noxious influences transmitted via placenta or breast milk, unspecified
KA07 - - Neonatal dermatoses due to maternal antibodies
KA07.0 - - - Neonatal lupus erythematosus
KA07.1 - - - Neonatal pemphigus
KA07.Y - - - Other specified neonatal dermatoses due to maternal antibodies
KA0Z - - Fetus or newborn affected by unspecified maternal factors or by complications of pregnancy, labour or delivery
- Disorders of newborn related to length of gestation or foetal growth
KA20 - - Disorders of newborn related to slow foetal growth or foetal malnutrition
KA20.0 - - - Small for gestational age
KA20.00 - - - - Small for gestational age, symmetrical
KA20.01 - - - - Small for gestational age, asymmetrical
KA20.0Z - - - - Small for gestational age, unspecified
KA20.1 - - - Intrauterine growth restriction
KA20.10 - - - - Asymmetrical intrauterine growth restriction
KA20.11 - - - - Symmetrical intrauterine growth restriction
KA20.12 - - - - Intrauterine growth restriction associated with small for gestational age
KA20.1Y - - - - Other specified intrauterine growth restriction
KA20.1Z - - - - Intrauterine growth restriction, unspecified
KA20.2 - - - Foetal intrauterine malnutrition without mention of small for gestational age
KA20.Y - - - Other specified disorders of newborn related to slow foetal growth or foetal malnutrition
KA20.Z - - - Disorders of newborn related to slow foetal growth or foetal malnutrition, unspecified
KA21 - - Disorders of newborn related to short gestation or low birth weight, not elsewhere classified
KA21.0 - - - Extremely low birth weight of newborn
KA21.00 - - - - Extremely low birth weight of newborn, 499g or less
KA21.01 - - - - Extremely low birth weight of newborn, 500-749g
KA21.02 - - - - Extremely low birth weight of newborn, 750-999g
KA21.0Z - - - - Extremely low birth weight of newborn, unspecified
KA21.1 - - - Very low birth weight of newborn
KA21.10 - - - - Very low birth weight of newborn, 1000-1249g
KA21.11 - - - - Very low birth weight of newborn, 1250-1499g
KA21.1Z - - - - Very low birth weight of newborn, unspecified
KA21.2 - - - Low birth weight of newborn
KA21.20 - - - - Low birth weight of newborn, 1500-1999g
KA21.21 - - - - Low birth weight of newborn, 2000-2499g
KA21.2Z - - - - Low birth weight of newborn, unspecified
KA21.3 - - - Extreme prematurity of newborn
KA21.30 - - - - Extreme prematurity of newborn, gestational age less than 22 completed weeks
KA21.31 - - - - Extreme prematurity of newborn, gestational age 22 completed weeks
KA21.32 - - - - Extreme prematurity of newborn, gestational age 23 completed weeks
KA21.33 - - - - Extreme prematurity of newborn, gestational age 24 completed weeks
KA21.34 - - - - Extreme prematurity of newborn, gestational age 25 completed weeks
KA21.35 - - - - Extreme prematurity of newborn, gestational age 26 completed weeks
KA21.36 - - - - Extreme prematurity of newborn, gestational age 27 completed weeks
KA21.3Z - - - - Extreme prematurity of newborn, unspecified
KA21.4 - - - Preterm newborn
KA21.40 - - - - Preterm newborn, gestational age 28 completed weeks
KA21.41 - - - - Preterm newborn, gestational age 29 completed weeks
KA21.42 - - - - Preterm newborn, gestational age 30 completed weeks
KA21.43 - - - - Preterm newborn, gestational age 31 completed weeks
KA21.44 - - - - Preterm newborn, gestational age 32 completed weeks
KA21.45 - - - - Preterm newborn, gestational age 33 completed weeks
KA21.46 - - - - Preterm newborn, gestational age 34 completed weeks
KA21.47 - - - - Preterm newborn, gestational age 35 completed weeks
KA21.48 - - - - Preterm newborn, gestational age 36 completed weeks
KA21.4Z - - - - Preterm newborn, unspecified
KA22 - - Disorders of newborn related to long gestation or high birth weight
KA22.0 - - - Exceptionally large newborn
KA22.1 - - - Large newborn for gestational age
KA22.2 - - - Post-term newborn
KA22.3 - - - Postmaturity syndrome
KA2Y - - Other specified disorders of newborn related to length of gestation or foetal growth
KA2Z - - Disorders of newborn related to length of gestation or foetal growth, unspecified
- Birth injury
KA40 - - Birth injury to central nervous system
KA40.0 - - - Intracranial laceration or haemorrhage due to birth injury
KA40.00 - - - - Subdural haemorrhage due to birth injury
KA40.01 - - - - Cerebral haemorrhage due to birth injury
KA40.02 - - - - Cerebellar haemorrhage due to birth injury
KA40.03 - - - - Intraventricular haemorrhage due to birth injury
KA40.04 - - - - Subarachnoid haemorrhage due to birth injury
KA40.05 - - - - Tentorial tear due to birth injury
KA40.06 - - - - Cerebellar contusion due to birth injury
KA40.07 - - - - Cerebral contusion due to birth injury
KA40.08 - - - - Extradural or epidural haemorrhage due to birth injury
KA40.0Y - - - - Other specified intracranial laceration or haemorrhage due to birth injury
KA40.0Z - - - - Intracranial laceration or haemorrhage due to birth injury, unspecified
KA40.1 - - - Cerebral oedema due to birth injury
KA40.2 - - - Birth injury to spine or spinal cord
KA40.3 - - - Birth injury to brainstem
KA40.Y - - - Other specified birth injury to central nervous system
KA40.Z - - - Birth injury to central nervous system, unspecified
KA41 - - Birth injury to eye
KA42 - - Birth injury to scalp
KA42.0 - - - Bruising of scalp due to birth injury
KA42.1 - - - Cephalohaematoma due to birth injury
KA42.2 - - - Chignon due to birth injury
KA42.3 - - - Monitoring injury of scalp of newborn
KA42.4 - - - Subgaleal epicranial subaponeurotic haemorrhage due to birth injury
KA42.Y - - - Other specified birth injury to scalp
KA43 - - Birth injury to skin or soft tissues
KA43.0 - - - Birth injury to sternocleidomastoid
KA43.1 - - - Birth injury to external genitalia
KA43.2 - - - Subcutaneous fat necrosis due to birth injury
KA43.3 - - - Birth injury to face
KA43.Y - - - Other specified birth injury to skin or soft tissues
KA44 - - Birth injury to peripheral nervous system
KA44.0 - - - Birth injury to cranial nerves
KA44.00 - - - - Birth injury to facial nerve
KA44.0Y - - - - Birth injury to other specified cranial nerve
KA44.0Z - - - - Birth injury to cranial nerves, unspecified
KA44.1 - - - Brachial plexus palsy in newborn
KA44.10 - - - - Erb paralysis
KA44.11 - - - - Klumpke paralysis
KA44.2 - - - Phrenic nerve paralysis due to birth injury
KA44.Y - - - Other specified birth injury to peripheral nervous system
KA45 - - Birth injury to skeleton
KA45.0 - - - Fracture of skull due to birth injury
KA45.00 - - - - Linear skull fracture due to birth injury
KA45.01 - - - - Depressed skull fracture due to birth injury
KA45.0Y - - - - Other specified fracture of skull due to birth injury
KA45.0Z - - - - Fracture of skull due to birth injury, unspecified
KA45.1 - - - Occipital osteodiastasis due to birth injury
KA45.2 - - - Birth injury to facial bones
KA45.20 - - - - Mandibular bone fracture due to birth injury
KA45.21 - - - - Nasal bone fracture due to birth injury
KA45.2Y - - - - Other specified birth injury to facial bones
KA45.2Z - - - - Birth injury to facial bones, unspecified
KA45.3 - - - Birth injury of thorax
KA45.4 - - - Fracture, dislocation or subluxation of spine due to birth injury
KA45.5 - - - Fracture of clavicle due to birth injury
KA45.6 - - - Birth injury to long bones
KA45.Y - - - Other specified birth injury to skeleton
KA46 - - Birth injury to other organs
KA46.0 - - - Birth injury to liver
KA46.1 - - - Birth injury to spleen
KA46.2 - - - Adrenal haemorrhage due to birth injury
KA46.Y - - - Birth injury to other specified organ
KA4Z - - Birth injury, unspecified
- Infections of the foetus or newborn
KA60 - - Sepsis of foetus or newborn
KA61 - - Other bacterial infections of the foetus or newborn
KA61.0 - - - Congenital tuberculosis
KA61.1 - - - Neonatal listeriosis
KA61.Z - - - Bacterial infection of the foetus or newborn, unspecified
KA62 - - Viral infection in the foetus or newborn
KA62.0 - - - Congenital Zika virus infection
KA62.1 - - - Congenital Epstein-Barr virus infection
KA62.2 - - - Congenital Varicella Zoster virus infection
KA62.3 - - - Congenital cytomegalovirus infection
KA62.4 - - - Congenital echovirus infection
KA62.5 - - - Congenital enterovirus infection
KA62.6 - - - Congenital human immunodeficiency virus infection
KA62.7 - - - Congenital parvovirus syndrome
KA62.8 - - - Congenital rubella syndrome
KA62.9 - - - Congenital viral hepatitis
KA62.A - - - Perinatal Herpes simplex infection
KA62.Y - - - Other specified viral infection in the foetus or newborn
KA62.Z - - - Viral infection in the foetus or newborn, unspecified
KA63 - - Fungal infection of foetus or newborn
KA63.0 - - - Malassezia infection in newborn
KA63.1 - - - Neonatal aspergillosis
KA63.2 - - - Neonatal candidosis
KA63.Y - - - Other specified fungal infection of foetus or newborn
KA63.Z - - - Fungal infection of foetus or newborn, unspecified
KA64 - - Parasitic diseases in the foetus or newborn
KA64.0 - - - Congenital toxoplasmosis
KA64.1 - - - Congenital falciparum malaria
KA64.Y - - - Other specified parasitic diseases in the foetus or newborn
KA64.Z - - - Parasitic diseases in the foetus or newborn, unspecified
KA65 - - Neonatal infections of certain specified sites
KA65.0 - - - Neonatal conjunctivitis or dacryocystitis
KA65.1 - - - Omphalitis of newborn
KA65.2 - - - Neonatal urinary tract infection
KA65.3 - - - Neonatal infectious mastitis
KA65.4 - - - Neonatal meningitis
KA65.Y - - - Neonatal infections of other specified sites
KA6Y - - Other specified infections of the foetus or newborn
KA6Z - - Infections of the foetus or newborn, unspecified
- Haemorrhagic or haematological disorders of foetus or newborn
KA80 - - Foetal blood loss
KA80.0 - - - Foetal blood loss from vasa praevia
KA80.1 - - - Foetal blood loss from ruptured cord
KA80.2 - - - Foetal blood loss from placenta
KA80.3 - - - Haemorrhage into co-twin
KA80.4 - - - Haemorrhage into maternal circulation
KA80.5 - - - Foetal blood loss from cut end of co-twin cord
KA80.Y - - - Other specified foetal blood loss
KA80.Z - - - Foetal blood loss, unspecified
KA81 - - Umbilical haemorrhage of newborn
KA82 - - Intracranial nontraumatic haemorrhage of foetus or newborn
KA82.0 - - - Intraventricular nontraumatic haemorrhage, grade 1, of foetus or newborn
KA82.1 - - - Intraventricular nontraumatic haemorrhage, grade 2, of foetus or newborn
KA82.2 - - - Intraventricular nontraumatic haemorrhage, grade 3, of foetus or newborn
KA82.3 - - - Intraventricular nontraumatic haemorrhage, grade 4, of foetus or newborn
KA82.4 - - - Intracerebral nontraumatic haemorrhage of foetus or newborn
KA82.5 - - - Subarachnoid nontraumatic haemorrhage of foetus or newborn
KA82.6 - - - Cerebellar nontraumatic, hemispheres or vermis or posterior fossa haemorrhage of foetus or newborn
KA82.7 - - - Subdural nontraumatic haemorrhage of foetus or newborn
KA82.Z - - - Intracranial nontraumatic haemorrhage of foetus or newborn, unspecified
KA83 - - Certain specified neonatal haemorrhages
KA83.0 - - - Neonatal bleeding originating in the mouth, nose or pharynx
KA83.1 - - - Neonatal bleeding originating in the oesophagus, stomach, small or large intestine
KA83.2 - - - Neonatal rectal haemorrhage
KA83.3 - - - Neonatal hepatic haemorrhage
KA83.4 - - - Neonatal haemorrhage originating in adrenal gland
KA83.5 - - - Neonatal haemorrhage originating in spleen
KA83.6 - - - Neonatal haemorrhage originating in kidney or bladder
KA83.7 - - - Neonatal haemorrhage originating in trachea or pulmonary parenchyma
KA83.8 - - - Neonatal cutaneous haemorrhage
KA83.9 - - - Neonatal vaginal or uterine haemorrhage
KA83.A - - - Neonatal epistaxis
KA84 - - Haemolytic disease of foetus or newborn
KA84.0 - - - Rh isoimmunization of foetus or newborn
KA84.1 - - - Isoimmunization due to other red cell factors
KA84.2 - - - ABO isoimmunization of foetus or newborn
KA84.3 - - - Haemolytic anaemia due to other unclassified antibodies
KA84.4 - - - Haemolytic disease due to disease of other neonatal organs
KA84.5 - - - Neonatal haemolysis due to systemic bacterial infection with or without concomitant diffuse intravascular coagulation
KA84.Z - - - Haemolytic disease of foetus or newborn, unspecified
KA85 - - Hydrops fetalis due to haemolytic disease
KA85.0 - - - Hydrops fetalis due to isoimmunization
KA85.Y - - - Other specified hydrops fetalis due to haemolytic disease
KA85.Z - - - Hydrops fetalis due to haemolytic disease, unspecified
KA86 - - Neonatal kernicterus
KA87 - - Neonatal hyperbilirubinaemia
KA87.0 - - - Neonatal hyperbilirubinaemia due to swallowed maternal blood
KA87.1 - - - Neonatal hyperbilirubinaemia due to enzymatic defect in bilirubin degradation
KA87.2 - - - Neonatal hyperbilirubinaemia due to breast milk inhibitor of bilirubin conjugation
KA87.3 - - - Neonatal hyperbilirubinaemia due to total parenteral nutrition
KA87.4 - - - Neonatal hyperbilirubinaemia due to drugs or toxins transmitted from mother
KA87.5 - - - Neonatal hyperbilirubinaemia due to drugs or toxins given to newborn
KA87.6 - - - Neonatal hyperbilirubinaemia from other or unspecified hepatocellular damage
KA87.Y - - - Other specified neonatal hyperbilirubinaemia
KA87.Z - - - Neonatal hyperbilirubinaemia, unspecified
KA88 - - Disseminated intravascular coagulation of foetus or newborn
KA89 - - Transient neonatal thrombocytopaenia
KA89.0 - - - Thrombocytopaenia following systemic infection, including diffuse intravascular coagulation
KA89.Y - - - Other specified transient neonatal thrombocytopaenia
KA89.Z - - - Transient neonatal thrombocytopaenia, unspecified
KA8A - - Polycythaemia neonatorum
KA8A.0 - - - Polycythaemia neonatorum due to placental insufficiency or foetal intrauterine growth restriction
KA8A.1 - - - Polycythemia neonatorum due to twin to twin transfusion
KA8A.2 - - - Polycythemia neonatorum due to inherited disorder of erythropoietin production
KA8A.3 - - - Polycythemia neonatorum following umbilical cord transfusion or stripping at delivery
KA8A.4 - - - Polycythemia neonatorum following blood transfusion
KA8A.Y - - - Other specified polycythaemia neonatorum
KA8A.Z - - - Polycythaemia neonatorum, unspecified
KA8B - - Anaemia of prematurity
KA8C - - Congenital hypoplastic anaemia
KA8D - - Transient neonatal neutropenia
KA8E - - Alloimmune neonatal neutropenia
KA8F - - Neonatal vitamin K deficiency
KA8F.0 - - - Diffuse bleeding diathesis due to vitamin K deficient haemorrhagic disease of foetus or newborn
KA8F.Y - - - Other specified neonatal vitamin K deficiency
KA8F.Z - - - Neonatal vitamin K deficiency, unspecified
KA8Y - - Other specified haemorrhagic or haematological disorders of foetus or newborn
KA8Z - - Haemorrhagic or haematological disorders of foetus or newborn, unspecified
- Neurological disorders specific to the perinatal or neonatal period
KB00 - - Neonatal cerebral ischaemia
KB00.0 - - - Perinatal arterial stroke
KB00.1 - - - Neonatal cerebral sinovenous thrombosis
KB00.Y - - - Other specified neonatal cerebral ischaemia
KB00.Z - - - Neonatal cerebral ischaemia, unspecified
KB01 - - Periventricular cysts of newborn
KB02 - - Neonatal cerebral leukomalacia
KB03 - - Neonatal encephalopathy
KB04 - - Hypoxic ischaemic encephalopathy of newborn
KB05 - - Neonatal hydrocephalus
KB05.0 - - - Neonatal obstructive hydrocephalus
KB05.Y - - - Other specified neonatal hydrocephalus
KB05.Z - - - Neonatal hydrocephalus, unspecified
KB06 - - Neonatal seizures
KB07 - - Compression of brain in neonate
KB08 - - Disorders of muscle tone of newborn
KB08.0 - - - Transient neonatal myasthenia gravis
KB08.1 - - - Congenital hypertonia
KB08.2 - - - Congenital hypotonia
KB08.Y - - - Other specified disorders of muscle tone of newborn
KB08.Z - - - Disorders of muscle tone of newborn, unspecified
KB0Y - - Other specified neurological disorders specific to the perinatal or neonatal period
KB0Z - - Neurological disorders specific to the perinatal or neonatal period, unspecified
- Respiratory disorders specific to the perinatal or neonatal period
KB20 - - Intrauterine hypoxia
KB20.0 - - - Intrauterine hypoxia first noted before onset of labour
KB20.1 - - - Intrauterine hypoxia first noted during labour or delivery
KB20.Z - - - Intrauterine hypoxia, unspecified
KB21 - - Birth asphyxia
KB21.0 - - - Severe birth asphyxia
KB21.1 - - - Mild and moderate birth asphyxia
KB21.Y - - - Other specified birth asphyxia
KB22 - - Metabolic acidaemia in newborn
KB23 - - Respiratory distress of newborn
KB23.0 - - - Respiratory distress syndrome of newborn
KB23.00 - - - - Respiratory distress syndrome of the newborn, altered by maternal corticosteroid therapy
KB23.01 - - - - Respiratory distress syndrome of the newborn, altered by pulmonary surfactant replacement therapy
KB23.02 - - - - Respiratory distress syndrome of the newborn, altered by maternal corticosteroid therapy or pulmonary surfactant replacement therapy
KB23.0Y - - - - Other specified respiratory distress syndrome of newborn
KB23.0Z - - - - Respiratory distress syndrome of newborn, unspecified
KB23.1 - - - Transient tachypnoea of newborn
KB23.2 - - - Respiratory instability of prematurity
KB23.Y - - - Other specified respiratory distress of newborn
KB23.Z - - - Respiratory distress of newborn, unspecified
KB24 - - Congenital pneumonia
KB25 - - Neonatal tracheitis
KB26 - - Neonatal aspiration syndromes
KB26.0 - - - Neonatal aspiration of meconium
KB26.1 - - - Neonatal aspiration of amniotic fluid or mucus
KB26.2 - - - Neonatal aspiration of blood
KB26.3 - - - Neonatal aspiration of milk or regurgitated food
KB26.Y - - - Other specified neonatal aspiration syndromes
KB26.Z - - - Neonatal aspiration syndromes, unspecified
KB27 - - Pulmonary air leak or related conditions originating in the perinatal period
KB27.0 - - - Interstitial emphysema originating in the perinatal period
KB27.1 - - - Pneumothorax originating in the perinatal period
KB27.2 - - - Pneumomediastinum originating in the perinatal period
KB27.3 - - - Pneumopericardium originating in the perinatal period
KB27.4 - - - Pneumoperitoneum, originating in the perinatal period, due to primary pulmonary air leak syndromes
KB27.Y - - - Other specified pulmonary air leak or related conditions originating in the perinatal period
KB27.Z - - - Pulmonary air leak or related conditions originating in the perinatal period, unspecified
KB28 - - Pulmonary haemorrhage originating in the perinatal period
KB28.0 - - - Tracheobronchial haemorrhage originating in the perinatal period
KB28.1 - - - Traumatic pulmonary haemorrhage originating in the perinatal period
KB28.Y - - - Other specified pulmonary haemorrhage originating in the perinatal period
KB28.Z - - - Pulmonary haemorrhage originating in the perinatal period, unspecified
KB29 - - Chronic respiratory disease originating in the perinatal period
KB29.0 - - - Bronchopulmonary dysplasia originating in the perinatal period
KB29.Y - - - Other specified chronic respiratory disease originating in the perinatal period
KB29.Z - - - Chronic respiratory disease originating in the perinatal period, unspecified
KB2A - - Apnoea of newborn
KB2A.0 - - - Central neonatal apnoea
KB2A.1 - - - Obstructive neonatal apnoea
KB2A.2 - - - Mixed neonatal apnoea
KB2A.3 - - - Apnoea of newborn, due to neurologic injury
KB2A.Y - - - Other specified apnoea of newborn
KB2A.Z - - - Apnoea of newborn, unspecified
KB2B - - Primary atelectasis of newborn
KB2C - - Cyanotic attacks of newborn
KB2D - - Respiratory failure of newborn
KB2E - - Respiratory arrest of newborn
KB2F - - Congenital lung or lobar atelectasis
KB2G - - Tracheal haemorrhage of newborn due to airway trauma
KB2H - - Acquired vocal cord paralysis in newborn
KB2J - - Airway obstruction in the neonate due to airway abnormality
KB2J.0 - - - Hypotonia of hypopharynx in neonate
KB2J.1 - - - Hypopharyngeal mass in neonate
KB2J.2 - - - Tracheo-bronchial malacia in neonate
KB2J.Y - - - Other specified airway obstruction in the neonate due to airway abnormality
KB2J.Z - - - Airway obstruction in the neonate due to airway abnormality, unspecified
KB2K - - Pulmonary cysts in newborn
KB2K.0 - - - Acquired pulmonary cysts in newborn
KB2K.Z - - - Pulmonary cysts in newborn, unspecified
KB2Y - - Other specified respiratory disorders specific to the perinatal or neonatal period
KB2Z - - Respiratory disorders specific to the perinatal or neonatal period, unspecified
- Cardiovascular disorders present in the perinatal or neonatal period
KB40 - - Neonatal cardiac failure
KB40.0 - - - Neonatal cardiac failure due to pulmonary overperfusion
KB40.1 - - - Neonatal cardiac failure due to decreased left ventricular output
KB40.Y - - - Other specified neonatal cardiac failure
KB40.Z - - - Neonatal cardiac failure, unspecified
KB41 - - Cardiac arrhythmias in the neonate
KB42 - - Persistent pulmonary hypertension of the newborn
KB43 - - Delayed closure of ductus arteriosus
KB44 - - Transient myocardial ischaemia of newborn
KB45 - - Neonatal hypertension
KB46 - - Neonatal hypotension
KB47 - - Benign or innocent cardiac murmurs in newborn
KB4Y - - Other specified cardiovascular disorders present in the perinatal or neonatal period
KB4Z - - Cardiovascular disorders present in the perinatal or neonatal period, unspecified
- Transitory endocrine or metabolic disorders specific to foetus or newborn
KB60 - - Transitory disorders of carbohydrate metabolism specific to foetus or newborn
KB60.0 - - - Syndrome of infant of mother with gestational diabetes
KB60.1 - - - Syndrome of infant of a diabetic mother, type I or II, nongestational, insulin dependent
KB60.2 - - - Neonatal diabetes mellitus
KB60.20 - - - - Transient neonatal diabetes mellitus
KB60.2Y - - - - Other specified neonatal diabetes mellitus
KB60.2Z - - - - Neonatal diabetes mellitus, unspecified
KB60.3 - - - Neonatal hyperglycemia
KB60.30 - - - - Neonatal hyperglycemia due to insulin deficiency
KB60.31 - - - - Neonatal hyperglycemia due to iatrogenic intravenous therapy
KB60.3Y - - - - Other specified neonatal hyperglycemia
KB60.3Z - - - - Neonatal hyperglycemia, unspecified
KB60.4 - - - Neonatal hypoglycaemia
KB60.40 - - - - Transient hyperinsulinemic neonatal hypoglycaemia
KB60.41 - - - - Transitory iatrogenic neonatal hypoglycaemia
KB60.42 - - - - Other transitory neonatal hypoglycaemia
KB60.4Y - - - - Other specified neonatal hypoglycaemia
KB60.4Z - - - - Neonatal hypoglycaemia, unspecified
KB60.Y - - - Other specified transitory disorders of carbohydrate metabolism specific to foetus or newborn
KB60.Z - - - Transitory disorders of carbohydrate metabolism specific to foetus or newborn, unspecified
KB61 - - Transitory neonatal disorders of calcium or magnesium metabolism
KB61.0 - - - Neonatal hypomagnesaemia
KB61.1 - - - Neonatal tetany without calcium or magnesium deficiency
KB61.2 - - - Neonatal hypocalcaemia
KB61.3 - - - Neonatal osteopenia
KB61.Y - - - Other specified transitory neonatal disorders of calcium or magnesium metabolism
KB61.Z - - - Transitory neonatal disorders of calcium or magnesium metabolism, unspecified
KB62 - - Transitory neonatal disorders of thyroid function
KB62.0 - - - Transitory neonatal hyperthyroidism
KB62.1 - - - Other transitory neonatal disorders of thyroid function, not elsewhere classified
KB62.2 - - - Transient hyperthyrotropinaemia
KB62.3 - - - Transient hypothyroxinaemia
KB62.Y - - - Other specified transitory neonatal disorders of thyroid function
KB62.Z - - - Transitory neonatal disorders of thyroid function, unspecified
KB63 - - Certain specified transitory neonatal electrolyte or metabolic disturbances
KB63.0 - - - Late metabolic acidosis of newborn
KB63.1 - - - Dehydration of newborn
KB63.2 - - - Disturbances of sodium balance of newborn
KB63.20 - - - - Hyponatremia of newborn
KB63.21 - - - - Hypernatremia of newborn
KB63.2Y - - - - Other specified disturbances of sodium balance of newborn
KB63.2Z - - - - Disturbances of sodium balance of newborn, unspecified
KB63.3 - - - Disturbances of potassium balance of newborn
KB63.30 - - - - Hypokalemia of newborn
KB63.31 - - - - Hyperkalemia of newborn
KB63.3Y - - - - Other specified disturbances of potassium balance of newborn
KB63.3Z - - - - Disturbances of potassium balance of newborn, unspecified
KB63.4 - - - Transitory tyrosinaemia of newborn
KB63.5 - - - Metabolic bone disease of prematurity
KB64 - - Transitory neonatal hypoparathyroidism
KB6Z - - Transitory endocrine or metabolic disorders specific to foetus or newborn, unspecified
- Digestive system disorders of foetus or newborn
KB80 - - Gastro-oesophageal reflux disease in newborn
KB81 - - Oesophagitis in newborn
KB81.0 - - - Neonatal eosinophilic oesophagitis
KB81.Y - - - Other specified oesophagitis in newborn
KB82 - - Prenatal gastric perforation
KB83 - - Postnatal gastric perforation
KB84 - - Postnatal isolated ileal perforation
KB85 - - Prenatal intrauterine intestinal perforation
KB85.0 - - - Prenatal intrauterine intestinal perforation due to in utero volvulus
KB85.1 - - - Prenatal intrauterine intestinal perforation due to intestinal atresia or stenosis
KB85.2 - - - Prenatal intrauterine intestinal perforation due to intraluminal obstruction
KB85.Y - - - Other specified prenatal intrauterine intestinal perforation
KB85.Z - - - Prenatal intrauterine intestinal perforation, unspecified
KB86 - - Postnatal intestinal perforation
KB86.0 - - - Postnatal intestinal perforation due to drugs
KB86.1 - - - Postnatal intestinal perforation due to in utero volvulus
KB86.2 - - - Postnatal intestinal perforation due to intestinal atresia or stenosis
KB86.3 - - - Postnatal intestinal perforation due to intraluminal obstruction
KB86.Y - - - Other specified postnatal intestinal perforation
KB86.Z - - - Postnatal intestinal perforation, unspecified
KB87 - - Intestinal obstruction of newborn
KB87.0 - - - Intestinal obstruction due to inspissated milk
KB87.1 - - - Meconium plug without ileus
KB87.2 - - - Meconium ileus without perforation
KB87.4 - - - Meconium ileus with perforation
KB87.3 - - - Transitory ileus of preterm-newborn
KB87.Y - - - Other specified intestinal obstruction of newborn
KB87.Z - - - Intestinal obstruction of newborn, unspecified
KB88 - - Necrotising enterocolitis of newborn
KB88.0 - - - Necrotising enterocolitis of newborn, Stage 1A & B
KB88.1 - - - Necrotising enterocolitis of newborn, Stage 2A & B
KB88.2 - - - Necrotising enterocolitis of newborn, Stage 3A
KB88.3 - - - Necrotising enterocolitis of newborn, Stage 3B
KB88.Y - - - Other specified necrotising enterocolitis of newborn
KB88.Z - - - Necrotising enterocolitis of newborn, unspecified
KB89 - - Neonatal malabsorption syndromes
KB89.0 - - - Neonatal malabsorption due to endocrine secreting tumour
KB89.1 - - - Short bowel syndrome
KB89.Y - - - Other specified neonatal malabsorption syndromes
KB89.Z - - - Neonatal malabsorption syndromes, unspecified
KB8A - - Neonatal haematemesis or melaena due to swallowed maternal blood
KB8B - - Neonatal peritonitis
KB8C - - Noninfectious neonatal diarrhoea
KB8Y - - Other specified digestive system disorders of foetus or newborn
KB8Z - - Digestive system disorders of foetus or newborn, unspecified
- Genitourinary system disorders specific to the perinatal or neonatal period
KC00 - - Congenital hydrocele
KC01 - - Congenital renal failure
KC0Y - - Other specified genitourinary system disorders specific to the perinatal or neonatal period
KC0Z - - Genitourinary system disorders specific to the perinatal or neonatal period, unspecified
- Disorders involving the integument of foetus or newborn
KC20 - - Conditions involving the umbilical cord
KC20.0 - - - Delayed separation of umbilical cord
KC20.1 - - - Umbilical cutis or polyp of newborn
KC20.2 - - - Umbilical granuloma of newborn
KC20.Y - - - Other specified conditions involving the umbilical cord
KC20.Z - - - Conditions involving the umbilical cord, unspecified
KC21 - - Inflammatory dermatoses of the newborn
KC21.0 - - - Neonatal acne
KC21.1 - - - Neonatal toxic erythema
KC21.2 - - - Perianal dermatitis of the newborn
KC21.Y - - - Other specified inflammatory dermatoses of the newborn
KC22 - - Neonatal disorders of subcutaneous fat
KC22.0 - - - Subcutaneous fat necrosis of the newborn
KC22.1 - - - Cold panniculitis of the newborn
KC22.2 - - - Sclerema neonatorum
KC22.Y - - - Other specified neonatal disorders of subcutaneous fat
KC23 - - Neonatal disorders of the oral mucosa
KC24 - - Neonatal nutritional disorders affecting the skin
- - Skin disorders associated with prematurity
KC30 - - - Skin fragility of prematurity
KC31 - - - Congenital erosive or vesicular dermatosis healing with reticulated supple scarring
KC3Y - - - Other specified skin disorders associated with prematurity
KC40 - - Miscellaneous skin disorders in the neonate
KC40.0 - - - Congenital sucking blisters
KC40.1 - - - Neonatal milia
KC40.Y - - - Other specified skin disorders in the neonate
KC41 - - Miscellaneous specified conditions of integument specific to foetus or newborn
KC41.0 - - - Breast engorgement of newborn
KC41.1 - - - Hydrops fetalis not due to haemolytic disease
KC41.Y - - - Other specified conditions of integument specific to fetus and newborn
- - Iatrogenic injuries involving the skin of the neonate
- - - Postnatal iatrogenic skin injury
KC50 - - - - Neonatal phototherapy burn
KC5Y - - - - Other specified postnatal iatrogenic skin injury
KC5Z - - - - Postnatal iatrogenic skin injury, unspecified
KC7Y - - - Other specified iatrogenic injuries involving the skin of the neonate
KC9Z - - Disorders involving the integument of foetus or newborn, unspecified
- Disturbances of temperature regulation of newborn
KD10 - - Environmental hyperthermia of newborn
KD11 - - Fever of newborn
KD12 - - Hypothermia of newborn
KD12.0 - - - Neonatal cold injury syndrome
KD12.Y - - - Other specified hypothermia of newborn
KD12.Z - - - Hypothermia of newborn, unspecified
KD1Y - - Other specified disturbances of temperature regulation of newborn
KD1Z - - Disturbances of temperature regulation of newborn, unspecified
- Certain disorders originating in the perinatal period
KD30 - - Birth depression
KD30.0 - - - Birth depression with 5 minute Apgar score 0-3
KD30.1 - - - Birth depression with 5 minute Apgar score 4-6
KD30.2 - - - Birth depression with associated metabolic acidaemia of cord blood
KD30.Z - - - Birth depression, unspecified
KD31 - - Wide cranial sutures of newborn
KD32 - - Feeding problems of newborn
KD32.0 - - - Slow feeding of newborn
KD32.1 - - - Underfeeding of newborn
KD32.2 - - - Overfeeding of newborn
KD32.3 - - - Neonatal difficulty in feeding at breast
KD32.4 - - - Failure to thrive in newborn
KD32.Y - - - Other specified feeding problems of newborn
KD32.Z - - - Feeding problems of newborn, unspecified
KD33 - - Jittery baby, not elsewhere classified
KD34 - - Reactions or intoxications due to drugs administered to foetus or newborn
KD35 - - Neonatal withdrawal syndrome from maternal use of drugs of addiction
KD36 - - Withdrawal symptoms from therapeutic use of drugs in newborn
KD37 - - Exposure to tobacco smoke in the perinatal period
KD38 - - Meconium staining
KD39 - - Complications of intrauterine procedures, not elsewhere classified
KD39.0 - - - Foetus or newborn affected by amniocentesis
KD39.1 - - - Foetus or newborn affected by chorionic villous sampling
KD39.2 - - - Foetus or newborn affected by foetal blood sampling
KD39.3 - - - Foetus or newborn affected by complications of foetal surgery
KD39.4 - - - Foetus or newborn affected by complications of intrauterine foetal surgery
KD39.Y - - - Other specified complications of intrauterine procedures, not elsewhere classified
KD39.Z - - - Complications of intrauterine procedures, not elsewhere classified, unspecified
KD3A - - Termination of pregnancy, affecting surviving foetus or newborn
KD3B - - Foetal death, cause not specified
KD3B.0 - - - Antepartum foetal death
KD3B.1 - - - Intrapartum foetal death
KD3B.Z - - - Unspecified time of fetal death, cause not specified
KD3C - - Vomiting in newborn
KD3C.0 - - - Bilious vomiting of newborn
KD3C.Y - - - Other specified vomiting in newborn
KD3C.Z - - - Vomiting in newborn, unspecified
KD3Y - - Other specified disorders originating in the perinatal period
KD5Z - Conditions originating in the perinatal or neonatal period, unspecified
Developmental anomalies
- Structural developmental anomalies primarily affecting one body system
- - Structural developmental anomalies of the nervous system
LA00 - - - Anencephaly or similar anomalies
LA00.0 - - - - Anencephaly
LA00.00 - - - - - Craniorachischisis
LA00.0Y - - - - - Other specified anencephaly
LA00.0Z - - - - - Anencephaly, unspecified
LA00.1 - - - - Iniencephaly
LA00.2 - - - - Acephaly
LA00.3 - - - - Amyelencephaly
LA00.Y - - - - Other specified anencephaly or similar anomalies
LA00.Z - - - - Anencephaly or similar anomalies, unspecified
LA01 - - - Cephalocele
LA02 - - - Spina bifida
LA02.0 - - - - Spina bifida cystica
LA02.00 - - - - - Myelomeningocele with hydrocephalus
LA02.01 - - - - - Myelomeningocele without hydrocephalus
LA02.02 - - - - - Myelocystocele
LA02.0Y - - - - - Other specified spina bifida cystica
LA02.0Z - - - - - Spina bifida cystica, unspecified
LA02.1 - - - - Spina bifida aperta
LA02.Y - - - - Other specified spina bifida
LA02.Z - - - - Spina bifida, unspecified
LA03 - - - Arnold-Chiari malformation type II
LA04 - - - Congenital hydrocephalus
LA04.0 - - - - Hydrocephalus with stenosis of the aqueduct of Sylvius
LA04.Y - - - - Other specified congenital hydrocephalus
LA04.Z - - - - Congenital hydrocephalus, unspecified
LA05 - - - Cerebral structural developmental anomalies
LA05.0 - - - - Microcephaly
LA05.1 - - - - Megalencephaly
LA05.2 - - - - Holoprosencephaly
LA05.3 - - - - Corpus callosum agenesis
LA05.4 - - - - Arhinencephaly
LA05.5 - - - - Abnormal neuronal migration
LA05.50 - - - - - Polymicrogyria
LA05.51 - - - - - Cortical dysplasia
LA05.5Y - - - - - Other specified abnormal neuronal migration
LA05.5Z - - - - - Abnormal neuronal migration, unspecified
LA05.6 - - - - Encephaloclastic disorders
LA05.60 - - - - - Porencephaly
LA05.61 - - - - - Schizencephaly
LA05.62 - - - - - Hydranencephaly
LA05.6Y - - - - - Other specified encephaloclastic disorders
LA05.6Z - - - - - Encephaloclastic disorders, unspecified
LA05.7 - - - - Brain cystic malformations
LA05.Y - - - - Other specified cerebral structural developmental anomalies
LA05.Z - - - - Cerebral structural developmental anomalies, unspecified
LA06 - - - Cerebellar structural developmental anomalies
LA06.0 - - - - Dandy-Walker malformation
LA06.1 - - - - Hypoplasia or agenesis of cerebellar hemispheres
LA06.2 - - - - Focal cerebellar dysplasia
LA06.Y - - - - Other specified cerebellar structural developmental anomalies
LA06.Z - - - - Cerebellar structural developmental anomalies, unspecified
LA07 - - - Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column
LA07.0 - - - - Primary tethered cord syndrome
LA07.1 - - - - Diastematomyelia
LA07.2 - - - - Amyelia
LA07.3 - - - - Primary syringomyelia or hydromyelia
LA07.4 - - - - Arnold-Chiari malformation type I
LA07.Y - - - - Other specified structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column
LA07.Z - - - - Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column, unspecified
LA0Y - - - Other specified structural developmental anomalies of the nervous system
LA0Z - - - Structural developmental anomalies of the nervous system, unspecified
- - Structural developmental anomalies of the eye, eyelid or lacrimal apparatus
LA10 - - - Structural developmental anomalies of ocular globes
LA10.0 - - - - Microphthalmos
LA10.1 - - - - Clinical anophthalmos
LA10.2 - - - - Buphthalmos
LA10.3 - - - - Congenital macrophthalmos
LA10.Y - - - - Other specified structural developmental anomalies of ocular globes
LA10.Z - - - - Structural developmental anomalies of ocular globes, unspecified
LA11 - - - Structural developmental anomalies of the anterior segment of eye
LA11.0 - - - - Blue sclera
LA11.1 - - - - Structural developmental anomalies of cornea
LA11.2 - - - - Anterior segment dysgenesis
LA11.3 - - - - Aniridia
LA11.4 - - - - Coloboma of iris
LA11.5 - - - - Congenital corneal opacity
LA11.6 - - - - Structural disorders of the pupil
LA11.60 - - - - - Irregular pupil of the eye
LA11.61 - - - - - Iridoschisis
LA11.62 - - - - - Anomalies of pupillary function
LA11.6Y - - - - - Other specified structural disorders of the pupil
LA11.6Z - - - - - Structural disorders of the pupil, unspecified
LA11.Y - - - - Other specified structural developmental anomalies of the anterior segment of eye
LA11.Z - - - - Structural developmental anomalies of the anterior segment of eye, unspecified
LA12 - - - Structural developmental anomalies of lens or zonula
LA12.0 - - - - Coloboma of lens
LA12.1 - - - - Congenital cataract
LA12.2 - - - - Congenital aphakia
LA12.3 - - - - Spherophakia
LA12.Y - - - - Other specified structural developmental anomalies of lens or zonula
LA12.Z - - - - Structural developmental anomalies of lens or zonula, unspecified
LA13 - - - Structural developmental anomalies of the posterior segment of eye
LA13.0 - - - - Congenital anomalies of the vitreous
LA13.1 - - - - Coloboma of choroid or retina
LA13.2 - - - - Coloboma of macula
LA13.3 - - - - Congenital vitreoretinal dysplasia
LA13.4 - - - - Optic pit
LA13.5 - - - - Congenital retinal aneurysm
LA13.6 - - - - Congenital malformations of choroid
LA13.7 - - - - Congenital malformation of optic disc
LA13.70 - - - - - Isolated optic nerve hypoplasia
LA13.71 - - - - - Optic nerve aplasia
LA13.72 - - - - - Congenitally elevated optic disc
LA13.73 - - - - - Optic disc dysplasia
LA13.74 - - - - - Megalopapilla
LA13.75 - - - - - Optic disc pit
LA13.76 - - - - - Coloboma of optic disc
LA13.7Y - - - - - Other specified congenital malformation of optic disc
LA13.7Z - - - - - Congenital malformation of optic disc, unspecified
LA13.8 - - - - Certain congenital malformations of posterior segment of eye
LA13.80 - - - - - Anastomosis of retinal or choroidal vessels
LA13.8Y - - - - - Other specified congenital malformations of posterior segment of eye
LA13.8Z - - - - - Certain congenital malformations of posterior segment of eye, unspecified
LA13.Y - - - - Other specified structural developmental anomalies of the posterior segment of eye
LA13.Z - - - - Structural developmental anomalies of the posterior segment of eye, unspecified
LA14 - - - Structural developmental anomalies of eyelid, lacrimal apparatus or orbit
LA14.0 - - - - Structural developmental anomalies of eyelids
LA14.00 - - - - - Palpebral cleft or coloboma
LA14.01 - - - - - Cryptophthalmia
LA14.02 - - - - - Congenital entropion
LA14.03 - - - - - Congenital ectropion
LA14.04 - - - - - Congenital ptosis
LA14.05 - - - - - Congenital eyelid retraction
LA14.06 - - - - - Epibulbar choristoma
LA14.07 - - - - - Ankyloblepharon filiforme adnatum
LA14.0Y - - - - - Other specified structural developmental anomalies of eyelids
LA14.1 - - - - Structural developmental anomalies of lacrimal apparatus
LA14.10 - - - - - Aplasia of lacrimal or salivary glands
LA14.11 - - - - - Agenesis of lacrimal ducts
LA14.12 - - - - - Congenital dacryocele
LA14.13 - - - - - Congenital agenesis of lacrimal punctum
LA14.14 - - - - - Congenital stenosis or stricture of lacrimal duct
LA14.1Y - - - - - Other specified structural developmental anomalies of lacrimal apparatus
LA14.1Z - - - - - Structural developmental anomalies of lacrimal apparatus, unspecified
LA14.2 - - - - Structural developmental anomalies of orbit
LA14.Y - - - - Other specified structural developmental anomalies of eyelid, lacrimal apparatus or orbit
LA14.Z - - - - Structural developmental anomalies of eyelid, lacrimal apparatus or orbit, unspecified
LA1Y - - - Other specified structural developmental anomalies of the eye, eyelid or lacrimal apparatus
LA1Z - - - Structural developmental anomalies of the eye, eyelid or lacrimal apparatus, unspecified
- - Structural developmental anomalies of the ear
LA20 - - - Structural anomaly of eustachian apparatus
LA21 - - - Minor anomalies of pinnae
LA21.0 - - - - Macrotia
LA21.1 - - - - Protruding ear
LA21.2 - - - - Low-set ear
LA21.3 - - - - Misshapen ear
LA21.Y - - - - Other specified minor anomalies of pinnae
LA22 - - - Structural developmental anomalies of ear causing hearing impairment
LA22.0 - - - - Microtia
LA22.1 - - - - Anotia
LA22.2 - - - - Aplasia or hypoplasia of external auditory canal
LA22.3 - - - - Structural developmental anomalies of ear ossicles
LA22.4 - - - - Structural developmental anomalies of inner ear
LA22.Y - - - - Other specified structural developmental anomalies of ear causing hearing impairment
LA22.Z - - - - Structural developmental anomalies of ear causing hearing impairment, unspecified
LA23 - - - Otocephaly
LA24 - - - Accessory auricle
LA2Y - - - Other specified structural developmental anomalies of the ear
LA2Z - - - Structural developmental anomalies of the ear, unspecified
- - Structural developmental anomalies of the face, mouth or teeth
LA30 - - - Structural developmental anomalies of teeth and periodontal tissues
LA30.0 - - - - Anodontia
LA30.1 - - - - Hypodontia
LA30.2 - - - - Oligodontia
LA30.3 - - - - Hyperdontia
LA30.4 - - - - Abnormalities of size or form of teeth
LA30.5 - - - - Anomalies in tooth resorption or loss
LA30.50 - - - - - Early exfoliation of teeth
LA30.51 - - - - - Late exfoliation of teeth
LA30.5Y - - - - - Other specified anomalies in tooth resorption or loss
LA30.5Z - - - - - Anomalies in tooth resorption or loss, unspecified
LA30.6 - - - - Amelogenesis imperfecta
LA30.7 - - - - Dentine dysplasia
LA30.8 - - - - Dentinogenesis imperfecta
LA30.9 - - - - Odontogenesis imperfecta
LA30.Y - - - - Other specified structural developmental anomalies of teeth and periodontal tissues
LA30.Z - - - - Structural developmental anomalies of teeth and periodontal tissues, unspecified
LA31 - - - Structural developmental anomalies of mouth or tongue
LA31.0 - - - - Congenital macroglossia
LA31.1 - - - - Hypoglossia or aglossia
LA31.2 - - - - Ankyloglossia
LA31.3 - - - - Macrostomia
LA31.4 - - - - Microstomia
LA31.Y - - - - Other specified structural developmental anomalies of mouth or tongue
- - - Clefts of lip, alveolus or palate
LA40 - - - - Cleft lip
LA40.0 - - - - - Cleft lip, unilateral
LA40.1 - - - - - Cleft lip, bilateral
LA40.2 - - - - - Cleft lip, median
LA40.Y - - - - - Other specified cleft lip
LA40.Z - - - - - Cleft lip, unspecified
LA41 - - - - Cleft lip and alveolus
LA41.0 - - - - - Cleft lip and alveolus, unilateral
LA41.1 - - - - - Cleft lip and alveolus, bilateral
LA41.Y - - - - - Other specified cleft lip and alveolus
LA41.Z - - - - - Cleft lip and alveolus, unspecified
LA42 - - - - Cleft palate
LA42.0 - - - - - Cleft hard palate
LA42.1 - - - - - Cleft soft palate
LA42.2 - - - - - Cleft uvula
LA42.Y - - - - - Other specified cleft palate
LA42.Z - - - - - Cleft palate, unspecified
LA4Y - - - - Other specified clefts of lip, alveolus or palate
LA4Z - - - - Clefts of lip, alveolus or palate, unspecified
LA50 - - - Congenital velopharyngeal incompetence
LA51 - - - Facial clefts
LA52 - - - Facial asymmetry
LA53 - - - Macrocheilia
LA54 - - - Microcheilia
LA55 - - - Compression facies
LA56 - - - Pierre Robin syndrome
LA5Y - - - Other specified structural developmental anomalies of the face, mouth or teeth
LA5Z - - - Structural developmental anomalies of the face, mouth or teeth, unspecified
- - Structural developmental anomalies of the neck
LA60 - - - Webbed neck
LA61 - - - Congenital sternomastoid tumour
LA62 - - - Congenital torticollis
LA6Y - - - Other specified structural developmental anomalies of the neck
LA6Z - - - Structural developmental anomalies of the neck, unspecified
- - Structural developmental anomalies of the respiratory system
LA70 - - - Structural developmental anomalies of the nose or cavum
LA70.0 - - - - Arrhinia
LA70.1 - - - - Bifid nose
LA70.2 - - - - Choanal atresia
LA70.3 - - - - Congenital perforated nasal septum
LA70.Y - - - - Other specified structural developmental anomalies of the nose or cavum
LA70.Z - - - - Structural developmental anomalies of the nose or cavum, unspecified
LA71 - - - Structural developmental anomalies of larynx
LA71.0 - - - - Congenital laryngomalacia
LA71.1 - - - - Laryngocele
LA71.2 - - - - Laryngeal hypoplasia
LA71.3 - - - - Congenital subglottic stenosis
LA71.Y - - - - Other specified structural developmental anomalies of larynx
LA71.Z - - - - Structural developmental anomalies of larynx, unspecified
LA72 - - - Laryngotracheooesophageal cleft
LA73 - - - Structural developmental anomalies of trachea
LA73.0 - - - - Congenital stenosis of trachea
LA73.1 - - - - Congenital tracheomalacia
LA73.Y - - - - Other specified structural developmental anomalies of trachea
LA73.Z - - - - Structural developmental anomalies of trachea, unspecified
LA74 - - - Structural developmental anomalies of bronchi
LA74.0 - - - - Congenital stenosis or atresia of bronchus
LA74.1 - - - - Congenital bronchomalacia
LA74.Y - - - - Other specified structural developmental anomalies of bronchi
LA74.Z - - - - Structural developmental anomalies of bronchi, unspecified
LA75 - - - Structural developmental anomalies of lungs
LA75.0 - - - - Accessory lobe of lung
LA75.1 - - - - Agenesis of lung
LA75.2 - - - - Congenital hypoplasia of lung
LA75.3 - - - - Congenital hyperplasia of lung
LA75.4 - - - - Congenital pulmonary airway malformations
LA75.5 - - - - Congenital lobar emphysema
LA75.6 - - - - Congenital sequestration of lung
LA75.Y - - - - Other specified structural developmental anomalies of lungs
LA75.Z - - - - Structural developmental anomalies of lungs, unspecified
LA76 - - - Structural developmental anomalies of pleura
LA77 - - - Congenital cyst of mediastinum
LA7Y - - - Other specified structural developmental anomalies of the respiratory system
LA7Z - - - Structural developmental anomalies of the respiratory system, unspecified
- - Structural developmental anomalies of the circulatory system
- - - Structural developmental anomaly of heart or great vessels
LA80 - - - - Anomalous position-orientation of heart
LA80.0 - - - - - Laevocardia
LA80.1 - - - - - Dextrocardia
LA80.2 - - - - - Mesocardia
LA80.3 - - - - - Extrathoracic heart
LA80.Y - - - - - Other specified anomalous position-orientation of heart
LA80.Z - - - - - Anomalous position-orientation of heart, unspecified
LA81 - - - - Abnormal ventricular relationships
LA82 - - - - Total mirror imagery
LA83 - - - - Right isomerism
LA84 - - - - Left isomerism
LA85 - - - - Congenital anomaly of an atrioventricular or ventriculo-arterial connection
LA85.0 - - - - - Discordant atrioventricular connections
LA85.1 - - - - - Transposition of the great arteries
LA85.2 - - - - - Double outlet right ventricle
LA85.20 - - - - - - Double outlet right ventricle with subpulmonary ventricular septal defect, transposition type
LA85.21 - - - - - - Double outlet right ventricle with non-committed ventricular septal defect
LA85.22 - - - - - - Double outlet right ventricle with subaortic or doubly committed ventricular septal defect without pulmonary stenosis, ventricular septal defect type
LA85.2Y - - - - - - Other specified double outlet right ventricle
LA85.2Z - - - - - - Double outlet right ventricle, unspecified
LA85.3 - - - - - Double outlet left ventricle
LA85.4 - - - - - Common arterial trunk
LA85.40 - - - - - - Common arterial trunk with aortic dominance
LA85.41 - - - - - - Common arterial trunk with pulmonary dominance and interrupted aortic arch
LA85.4Y - - - - - - Other specified common arterial trunk
LA85.4Z - - - - - - Common arterial trunk, unspecified
LA85.Y - - - - - Other specified congenital anomaly of an atrioventricular or ventriculo-arterial connection
LA85.Z - - - - - Congenital anomaly of an atrioventricular or ventriculo-arterial connection, unspecified
LA86 - - - - Congenital anomaly of mediastinal vein
LA86.0 - - - - - Left superior caval vein
LA86.1 - - - - - Unroofed coronary sinus
LA86.2 - - - - - Anomalous pulmonary venous connection
LA86.20 - - - - - - Total anomalous pulmonary venous connection
LA86.21 - - - - - - Partial anomalous pulmonary venous connection
LA86.22 - - - - - - Scimitar syndrome
LA86.2Y - - - - - - Other specified anomalous pulmonary venous connection
LA86.2Z - - - - - - Anomalous pulmonary venous connection, unspecified
LA86.3 - - - - - Congenital pulmonary venous stenosis or hypoplasia
LA86.Y - - - - - Other specified congenital anomaly of mediastinal vein
LA86.Z - - - - - Congenital anomaly of mediastinal vein, unspecified
LA87 - - - - Congenital anomaly of an atrioventricular valve or atrioventricular septum
LA87.0 - - - - - Congenital anomaly of tricuspid valve
LA87.00 - - - - - - Congenital tricuspid regurgitation
LA87.01 - - - - - - Congenital tricuspid valvar stenosis
LA87.02 - - - - - - Dysplasia of tricuspid valve
LA87.03 - - - - - - Ebstein malformation of tricuspid valve
LA87.0Y - - - - - - Other specified congenital anomaly of tricuspid valve
LA87.0Z - - - - - - Congenital anomaly of tricuspid valve, unspecified
LA87.1 - - - - - Congenital anomaly of mitral valve
LA87.10 - - - - - - Congenital mitral regurgitation
LA87.11 - - - - - - Congenital mitral valvar stenosis
LA87.12 - - - - - - Dysplasia of mitral valve
LA87.13 - - - - - - Congenital anomaly of mitral subvalvar apparatus
LA87.1Y - - - - - - Other specified congenital anomaly of mitral valve
LA87.1Z - - - - - - Congenital anomaly of mitral valve, unspecified
LA87.2 - - - - - Common atrioventricular junction
LA87.20 - - - - - - Atrioventricular septal defect
LA87.2Y - - - - - - Other specified common atrioventricular junction
LA87.2Z - - - - - - Common atrioventricular junction, unspecified
LA87.Y - - - - - Other specified congenital anomaly of an atrioventricular valve or atrioventricular septum
LA87.Z - - - - - Congenital anomaly of an atrioventricular valve or atrioventricular septum, unspecified
LA88 - - - - Congenital anomaly of a ventricle or the ventricular septum
LA88.0 - - - - - Congenital right ventricular outflow tract obstruction
LA88.1 - - - - - Double chambered right ventricle
LA88.2 - - - - - Tetralogy of Fallot
LA88.20 - - - - - - Tetralogy of Fallot with absent pulmonary valve syndrome
LA88.21 - - - - - - Tetralogy of Fallot with pulmonary atresia
LA88.22 - - - - - - Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral artery
LA88.2Y - - - - - - Other specified tetralogy of Fallot
LA88.2Z - - - - - - Tetralogy of Fallot, unspecified
LA88.3 - - - - - Congenital left ventricular outflow tract obstruction
LA88.4 - - - - - Ventricular septal defect
LA88.40 - - - - - - Trabecular muscular ventricular septal defect
LA88.41 - - - - - - Perimembranous central ventricular septal defect
LA88.42 - - - - - - Ventricular septal defect haemodynamically insignificant
LA88.4Y - - - - - - Other specified ventricular septal defect
LA88.4Z - - - - - - Ventricular septal defect, unspecified
LA88.Y - - - - - Other specified congenital anomaly of a ventricle or the ventricular septum
LA88.Z - - - - - Congenital anomaly of a ventricle or the ventricular septum, unspecified
LA89 - - - - Functionally univentricular heart
LA89.0 - - - - - Double inlet atrioventricular connection
LA89.1 - - - - - Tricuspid atresia
LA89.2 - - - - - Mitral atresia
LA89.3 - - - - - Hypoplastic left heart syndrome
LA89.Y - - - - - Other specified functionally univentricular heart
LA89.Z - - - - - Functionally univentricular heart, unspecified
LA8A - - - - Congenital anomaly of a ventriculo-arterial valve or adjacent regions
LA8A.0 - - - - - Congenital anomaly of pulmonary valve
LA8A.00 - - - - - - Congenital pulmonary valvar stenosis
LA8A.01 - - - - - - Congenital pulmonary regurgitation
LA8A.0Y - - - - - - Other specified congenital anomaly of pulmonary valve
LA8A.0Z - - - - - - Congenital anomaly of pulmonary valve, unspecified
LA8A.1 - - - - - Congenital pulmonary atresia
LA8A.10 - - - - - - Pulmonary atresia with intact ventricular septum
LA8A.1Y - - - - - - Other specified congenital pulmonary atresia
LA8A.1Z - - - - - - Congenital pulmonary atresia, unspecified
LA8A.2 - - - - - Congenital anomaly of aortic valve
LA8A.20 - - - - - - Congenital aortic valvar stenosis
LA8A.21 - - - - - - Congenital aortic regurgitation
LA8A.22 - - - - - - Bicuspid aortic valve
LA8A.23 - - - - - - Aortic valvar atresia
LA8A.24 - - - - - - Unicuspid aortic valve
LA8A.2Y - - - - - - Other specified congenital anomaly of aortic valve
LA8A.2Z - - - - - - Congenital anomaly of aortic valve, unspecified
LA8A.3 - - - - - Congenital supravalvar aortic stenosis
LA8A.4 - - - - - Aneurysm of aortic sinus of Valsalva
LA8A.5 - - - - - Congenital subaortic stenosis
LA8A.6 - - - - - Congenital subpulmonary stenosis
LA8A.Y - - - - - Other specified congenital anomaly of a ventriculo-arterial valve or adjacent regions
LA8A.Z - - - - - Congenital anomaly of a ventriculo-arterial valve or adjacent regions, unspecified
LA8B - - - - Congenital anomaly of great arteries including arterial duct
LA8B.0 - - - - - Congenital aortopulmonary window
LA8B.1 - - - - - Congenital anomaly of pulmonary arterial tree
LA8B.2 - - - - - Congenital anomaly of aorta or its branches
LA8B.20 - - - - - - Congenital anomaly of descending thoracic or abdominal aorta
LA8B.21 - - - - - - Coarctation of aorta
LA8B.22 - - - - - - Interrupted aortic arch
LA8B.2Y - - - - - - Other specified congenital anomaly of aorta or its branches
LA8B.2Z - - - - - - Congenital anomaly of aorta or its branches, unspecified
LA8B.3 - - - - - Tracheo-oesophageal compressive syndrome
LA8B.4 - - - - - Patent arterial duct
LA8B.Y - - - - - Other specified congenital anomaly of great arteries including arterial duct
LA8B.Z - - - - - Congenital anomaly of great arteries including arterial duct, unspecified
LA8C - - - - Congenital anomaly of coronary arteries
LA8C.0 - - - - - Anomalous origin of coronary artery from pulmonary arterial tree
LA8C.1 - - - - - Anomalous aortic origin or course of coronary artery
LA8C.2 - - - - - Congenital coronary arterial fistula
LA8C.Y - - - - - Other specified congenital anomaly of coronary arteries
LA8C.Z - - - - - Congenital anomaly of coronary arteries, unspecified
LA8D - - - - Congenital pericardial anomaly
LA8E - - - - Congenital anomaly of atrial septum
LA8E.0 - - - - - Patent oval foramen
LA8E.1 - - - - - Atrial septal defect within oval fossa
LA8E.2 - - - - - Sinus venosus defect
LA8E.3 - - - - - Interatrial communication through coronary sinus orifice
LA8E.Y - - - - - Other specified congenital anomaly of atrial septum
LA8E.Z - - - - - Congenital anomaly of atrial septum, unspecified
LA8F - - - - Congenital anomaly of right atrium
LA8G - - - - Congenital anomaly of left atrium
LA8G.0 - - - - - Divided left atrium
LA8G.Y - - - - - Other specified congenital anomaly of left atrium
LA8G.Z - - - - - Congenital anomaly of left atrium, unspecified
LA8Y - - - - Other specified structural developmental anomaly of heart or great vessels
LA8Z - - - - Structural developmental anomaly of heart or great vessels, unspecified
LA90 - - - Structural developmental anomalies of the peripheral vascular system
LA90.0 - - - - Capillary malformations
LA90.00 - - - - - Hereditary haemorrhagic telangiectasia
LA90.0Y - - - - - Other specified capillary malformations
LA90.0Z - - - - - Capillary malformations, unspecified
LA90.1 - - - - Lymphatic malformations
LA90.10 - - - - - Macrocystic lymphatic malformation
LA90.11 - - - - - Microcystic lymphatic malformation
LA90.12 - - - - - Lymphatic malformations of certain specified sites
LA90.13 - - - - - Cystic hygroma in foetus
LA90.1Y - - - - - Other specified lymphatic malformations
LA90.1Z - - - - - Lymphatic malformations, unspecified
LA90.2 - - - - Peripheral venous malformations
LA90.20 - - - - - Vein of Galen aneurysm
LA90.21 - - - - - Anomalous portal venous connection
LA90.2Y - - - - - Other specified peripheral venous malformations
LA90.2Z - - - - - Peripheral venous malformations, unspecified
LA90.3 - - - - Peripheral arteriovenous malformations
LA90.30 - - - - - Portal vein-hepatic artery fistula
LA90.31 - - - - - Arteriovenous malformation of precerebral vessels
LA90.32 - - - - - Uterine arteriovenous malformations
LA90.3Y - - - - - Other specified peripheral arteriovenous malformations
LA90.3Z - - - - - Peripheral arteriovenous malformations, unspecified
LA90.4 - - - - Peripheral arterial malformations
LA90.40 - - - - - Congenital renal artery stenosis
LA90.41 - - - - - Congenital precerebral nonruptured aneurysm
LA90.42 - - - - - Congenital cerebral nonruptured aneurysm
LA90.4Y - - - - - Other specified peripheral arterial malformations
LA90.4Z - - - - - Peripheral arterial malformations, unspecified
LA90.5 - - - - Pulmonary arteriovenous fistula
LA90.Y - - - - Other specified structural developmental anomalies of the peripheral vascular system
LA90.Z - - - - Structural developmental anomalies of the peripheral vascular system, unspecified
LA9Y - - - Other specified structural developmental anomalies of the circulatory system
LA9Z - - - Structural developmental anomalies of the circulatory system, unspecified
- - Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord
LB00 - - - Structural developmental anomalies of diaphragm
LB00.0 - - - - Congenital diaphragmatic hernia
LB00.1 - - - - Absence of diaphragm
LB00.Y - - - - Other specified structural developmental anomalies of diaphragm
LB00.Z - - - - Structural developmental anomalies of diaphragm, unspecified
LB01 - - - Omphalocele
LB02 - - - Gastroschisis
LB03 - - - Structural developmental anomalies of umbilical cord
LB03.0 - - - - Allantoic duct remnants or cysts
LB03.1 - - - - Single umbilical cord artery
LB03.Y - - - - Other specified structural developmental anomalies of umbilical cord
LB03.Z - - - - Structural developmental anomalies of umbilical cord, unspecified
LB0Y - - - Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord
LB0Z - - - Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord, unspecified
- - Structural developmental anomalies of the digestive tract
LB10 - - - Structural developmental anomalies of salivary glands or ducts
LB11 - - - Congenital diverticulum of pharynx
LB12 - - - Structural developmental anomalies of oesophagus
LB12.0 - - - - Congenital oesophageal web or ring
LB12.1 - - - - Atresia of oesophagus
LB12.10 - - - - - Atresia of oesophagus with oesophagobronchial fistula
LB12.1Y - - - - - Other specified atresia of oesophagus
LB12.1Z - - - - - Atresia of oesophagus, unspecified
LB12.2 - - - - Oesophageal fistula without atresia
LB12.3 - - - - Congenital stenosis or stricture of oesophagus
LB12.4 - - - - Congenital diverticulum of oesophagus
LB12.5 - - - - Congenital dilatation of oesophagus
LB12.Y - - - - Other specified structural developmental anomalies of oesophagus
LB12.Z - - - - Structural developmental anomalies of oesophagus, unspecified
LB13 - - - Structural developmental anomalies of stomach
LB13.0 - - - - Congenital hypertrophic pyloric stenosis
LB13.1 - - - - Congenital hiatus hernia
LB13.2 - - - - Congenital antral web
LB13.Y - - - - Other specified structural developmental anomalies of stomach
LB13.Z - - - - Structural developmental anomalies of stomach, unspecified
LB14 - - - Structural developmental anomalies of duodenum
LB15 - - - Structural developmental anomalies of small intestine
LB15.0 - - - - Meckel diverticulum
LB15.1 - - - - Atresia of small intestine
LB15.2 - - - - Congenital short bowel
LB15.3 - - - - Congenital diverticulitis of small intestine
LB15.4 - - - - Congenital diverticulosis of small intestine
LB15.5 - - - - Congenital diverticulum of small intestine
LB15.Y - - - - Other specified structural developmental anomalies of small intestine
LB15.Z - - - - Structural developmental anomalies of small intestine, unspecified
LB16 - - - Structural developmental anomalies of large intestine
LB16.0 - - - - Congenital absence, atresia or stenosis of large intestine
LB16.1 - - - - Hirschsprung disease
LB16.2 - - - - Immature ganglionosis of large intestine
LB16.3 - - - - Congenital hypoganglionosis of large intestine
LB16.Y - - - - Other specified structural developmental anomalies of large intestine
LB16.Z - - - - Structural developmental anomalies of large intestine, unspecified
LB17 - - - Structural developmental anomalies of anal canal
LB17.0 - - - - Anorectal malformations
LB17.1 - - - - Ectopic anus
LB17.2 - - - - Persistent cloaca
LB17.3 - - - - Cloacal exstrophy
LB17.4 - - - - Perineal groove
LB17.Y - - - - Other specified structural developmental anomalies of anal canal
LB17.Z - - - - Structural developmental anomalies of anal canal, unspecified
LB18 - - - Congenital anomalies of intestinal fixation
LB1Y - - - Other specified structural developmental anomalies of the digestive tract
LB1Z - - - Structural developmental anomalies of the digestive tract, unspecified
- - Structural developmental anomalies of the liver, biliary tract, pancreas or spleen
LB20 - - - Structural developmental anomalies of gallbladder, bile ducts or liver
LB20.0 - - - - Structural developmental anomalies of liver
LB20.00 - - - - - Fibropolycystic liver disease
LB20.0Y - - - - - Other specified structural developmental anomalies of liver
LB20.0Z - - - - - Structural developmental anomalies of liver, unspecified
LB20.1 - - - - Structural developmental anomalies of gallbladder
LB20.10 - - - - - Agenesis, aplasia or hypoplasia of gallbladder
LB20.1Y - - - - - Other specified structural developmental anomalies of gallbladder
LB20.1Z - - - - - Structural developmental anomalies of gallbladder, unspecified
LB20.2 - - - - Structural developmental anomalies of bile ducts
LB20.20 - - - - - Choledochal cyst
LB20.21 - - - - - Biliary atresia
LB20.22 - - - - - Congenital stenosis or stricture of bile ducts
LB20.23 - - - - - Structural developmental anomalies of cystic duct
LB20.24 - - - - - Accessory bile duct
LB20.2Y - - - - - Other specified structural developmental anomalies of bile ducts
LB20.2Z - - - - - Structural developmental anomalies of bile ducts, unspecified
LB20.Y - - - - Other specified structural developmental anomalies of gallbladder, bile ducts or liver
LB20.Z - - - - Structural developmental anomalies of gallbladder, bile ducts or liver, unspecified
LB21 - - - Structural developmental anomalies of pancreas
LB21.0 - - - - Annular pancreas
LB21.1 - - - - Pancreas divisum
LB21.2 - - - - Accessory pancreas
LB21.3 - - - - Agenesis-aplasia of pancreas
LB21.4 - - - - Partial agenesis of pancreas
LB21.5 - - - - Hypoplasia of pancreas
LB21.Y - - - - Other specified structural developmental anomalies of pancreas
LB21.Z - - - - Structural developmental anomalies of pancreas, unspecified
LB22 - - - Structural developmental anomalies of spleen
LB22.0 - - - - Congenital asplenia
LB22.1 - - - - Polysplenia
LB22.2 - - - - Ectopic spleen
LB22.Y - - - - Other specified structural developmental anomalies of spleen
LB22.Z - - - - Structural developmental anomalies of spleen, unspecified
LB2Y - - - Other specified structural developmental anomalies of the liver, biliary tract, pancreas or spleen
LB2Z - - - Structural developmental anomalies of the liver, biliary tract, pancreas or spleen, unspecified
- - Structural developmental anomalies of the urinary system
LB30 - - - Structural developmental anomalies of kidneys
LB30.0 - - - - Renal agenesis or other reduction defects of kidney
LB30.00 - - - - - Renal agenesis
LB30.0Y - - - - - Other specified renal agenesis or other reduction defects of kidney
LB30.0Z - - - - - Renal agenesis or other reduction defects of kidney, unspecified
LB30.1 - - - - Renal dysplasia
LB30.2 - - - - Congenital single renal cyst
LB30.3 - - - - Renal tubular dysgenesis
LB30.4 - - - - Oligomeganephronia
LB30.5 - - - - Accessory kidney
LB30.6 - - - - Fusion anomaly of kidneys
LB30.60 - - - - - Lobulated kidney
LB30.61 - - - - - Fused pelvic kidney
LB30.62 - - - - - Horseshoe kidney
LB30.6Y - - - - - Other specified fusion anomaly of kidneys
LB30.6Z - - - - - Fusion anomaly of kidneys, unspecified
LB30.7 - - - - Ectopic or pelvic kidney
LB30.8 - - - - Medullary sponge kidney
LB30.9 - - - - Multicystic renal dysplasia
LB30.Y - - - - Other specified structural developmental anomalies of kidneys
LB30.Z - - - - Structural developmental anomalies of kidneys, unspecified
LB31 - - - Structural developmental anomalies of urinary tract
LB31.0 - - - - Congenital hydronephrosis
LB31.1 - - - - Congenital primary megaureter
LB31.2 - - - - Foetal lower urinary tract obstruction
LB31.3 - - - - Exstrophy of urinary bladder
LB31.4 - - - - Congenital diverticulum of urinary bladder
LB31.5 - - - - Duplication of urethra
LB31.6 - - - - Congenital megalourethra
LB31.7 - - - - Megacystis-megaureter
LB31.8 - - - - Atresia or stenosis of ureter
LB31.9 - - - - Agenesis of ureter
LB31.A - - - - Duplication of ureter
LB31.B - - - - Malposition of ureter
LB31.C - - - - Congenital absence of bladder or urethra
LB31.D - - - - Congenital vesico-uretero-renal reflux
LB31.Y - - - - Other specified structural developmental anomalies of urinary tract
LB31.Z - - - - Structural developmental anomalies of urinary tract, unspecified
LB3Y - - - Other specified structural developmental anomalies of the urinary system
LB3Z - - - Structural developmental anomalies of the urinary system, unspecified
- - Structural developmental anomalies of the female genital system
LB40 - - - Structural developmental anomalies of vulva
LB40.0 - - - - Absence of vulva
LB40.1 - - - - Embryonic cyst of vulva
LB40.2 - - - - Fusion of labia
LB40.Y - - - - Other specified structural developmental anomalies of vulva
LB40.Z - - - - Structural developmental anomalies of vulva, unspecified
LB41 - - - Structural developmental anomalies of clitoris
LB41.0 - - - - Agenesis of clitoris
LB41.1 - - - - Duplication of clitoris
LB41.2 - - - - Clitoromegaly
LB41.Y - - - - Other specified structural developmental anomalies of clitoris
LB41.Z - - - - Structural developmental anomalies of clitoris, unspecified
LB42 - - - Structural developmental anomalies of vagina
LB42.0 - - - - Absence of vagina
LB42.1 - - - - Septate vagina
LB42.2 - - - - Congenital rectovaginal fistula
LB42.3 - - - - Tight hymenal ring
LB42.4 - - - - Imperforate hymen
LB42.5 - - - - Stricture or atresia of vagina
LB42.Y - - - - Other specified structural developmental anomalies of vagina
LB42.Z - - - - Structural developmental anomalies of vagina, unspecified
LB43 - - - Structural developmental anomalies of cervix uteri
LB43.0 - - - - Embryonic cyst of cervix
LB43.1 - - - - Agenesis or aplasia of cervix
LB43.Y - - - - Other specified structural developmental anomalies of cervix uteri
LB43.Z - - - - Structural developmental anomalies of cervix uteri, unspecified
LB44 - - - Structural developmental anomalies of uterus, except cervix
LB44.0 - - - - Agenesis or aplasia of uterine body
LB44.1 - - - - Hypoplasia of uterus
LB44.2 - - - - Unicornuate uterus
LB44.3 - - - - Bicornuate uterus
LB44.4 - - - - Septate uterus
LB44.5 - - - - Congenital fistulae between uterus and digestive and urinary tracts
LB44.6 - - - - Uterovaginal malformation due to diethylstilbestrol syndrome
LB44.Y - - - - Other specified structural developmental anomalies of uterus, except cervix
LB44.Z - - - - Structural developmental anomalies of uterus, except cervix, unspecified
LB45 - - - Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments
LB45.0 - - - - Congenital absence of ovary
LB45.1 - - - - 46,XX gonadal dysgenesis
LB45.2 - - - - Developmental ovarian cyst
LB45.3 - - - - Congenital torsion of ovary
LB45.4 - - - - Accessory ovary
LB45.5 - - - - Congenital absence of fallopian tube
LB45.6 - - - - Atresia of fallopian tube
LB45.7 - - - - Accessory fallopian tube
LB45.8 - - - - Embryonic cyst of fallopian tube
LB45.9 - - - - Embryonic cyst of broad ligament
LB45.Y - - - - Other specified structural developmental anomalies of ovaries, fallopian tubes or broad ligaments
LB45.Z - - - - Structural developmental anomalies of ovaries, fallopian tubes or broad ligaments, unspecified
LB4Y - - - Other specified structural developmental anomalies of the female genital system
LB4Z - - - Structural developmental anomalies of the female genital system, unspecified
- - Structural developmental anomalies of the male genital system
LB50 - - - Micropenis or penis agenesis
LB51 - - - Anorchia or microorchidia
LB52 - - - Cryptorchidism
LB52.0 - - - - Ectopic testis
LB52.1 - - - - Undescended testicle, unilateral
LB52.2 - - - - Undescended testicle, bilateral
LB52.Y - - - - Other specified cryptorchidism
LB52.Z - - - - Cryptorchidism, unspecified
LB53 - - - Hypospadias
LB53.0 - - - - Hypospadias, balanic
LB53.00 - - - - - Hypospadias, coronal
LB53.01 - - - - - Hypospadias, glandular
LB53.0Y - - - - - Other specified hypospadias, balanic
LB53.0Z - - - - - Hypospadias, balanic, unspecified
LB53.1 - - - - Hypospadias, penile
LB53.2 - - - - Hypospadias, penoscrotal
LB53.3 - - - - Hypospadias, scrotal
LB53.4 - - - - Hypospadias, perineal
LB53.Y - - - - Other specified hypospadias
LB53.Z - - - - Hypospadias, unspecified
LB54 - - - Congenital chordee
LB55 - - - Epispadias
LB56 - - - Bifid scrotum
LB57 - - - Agenesis of vas deferens
LB58 - - - Polyorchidism
LB59 - - - Hypoplasia of testis or scrotum
LB5Y - - - Other specified structural developmental anomalies of the male genital system
LB5Z - - - Structural developmental anomalies of the male genital system, unspecified
- - Structural developmental anomalies of the breast
LB60 - - - Breast aplasia
LB61 - - - Absent nipple
LB62 - - - Supernumerary breasts
LB63 - - - Accessory nipple
LB6Y - - - Other specified structural developmental anomalies of the breast
LB6Z - - - Structural developmental anomalies of the breast, unspecified
- - Structural developmental anomalies of the skeleton
LB70 - - - Structural developmental anomalies of cranium
LB70.0 - - - - Craniosynostosis
LB70.00 - - - - - Plagiocephaly
LB70.0Y - - - - - Other specified craniosynostosis
LB70.0Z - - - - - Craniosynostosis, unspecified
LB70.1 - - - - Wormian bones
LB70.2 - - - - J-shaped sella turcica
LB70.3 - - - - Macrocephaly
LB70.Y - - - - Other specified structural developmental anomalies of cranium
LB70.Z - - - - Structural developmental anomalies of cranium, unspecified
LB71 - - - Structural developmental anomalies of facial bones
LB71.0 - - - - Hypotelorism
LB71.1 - - - - Hypertelorism
LB71.Y - - - - Other specified structural developmental anomalies of facial bones
LB71.Z - - - - Structural developmental anomalies of facial bones, unspecified
LB72 - - - Structural developmental anomalies of shoulder girdle
LB72.0 - - - - Cervical rib
LB72.1 - - - - Sprengel deformity
LB72.2 - - - - Deformation of scapula
LB72.Y - - - - Other specified structural developmental anomalies of shoulder girdle
LB72.Z - - - - Structural developmental anomalies of shoulder girdle, unspecified
LB73 - - - Structural developmental anomalies of spine or bony thorax
LB73.0 - - - - Occult spinal dysraphism
LB73.1 - - - - Structural developmental anomalies of chest wall
LB73.10 - - - - - Poland syndrome
LB73.11 - - - - - Bifid rib
LB73.12 - - - - - Accessory rib
LB73.13 - - - - - Structural developmental anomalies of sternum
LB73.1Y - - - - - Other specified structural developmental anomalies of chest wall
LB73.1Z - - - - - Structural developmental anomalies of chest wall, unspecified
LB73.2 - - - - Structural developmental anomalies of spine
LB73.20 - - - - - Klippel-Feil anomaly
LB73.21 - - - - - Occipitalisation of atlas
LB73.22 - - - - - Atlanto-axial instability or subluxation
LB73.23 - - - - - Aplasia or hypoplasia of the odontoid process of axis
LB73.24 - - - - - Segmentation anomalies of vertebrae
LB73.25 - - - - - Congenital scoliosis due to congenital bony malformation
LB73.26 - - - - - Sacralization of the last lumbar vertebra
LB73.27 - - - - - Lumbarisation of the first sacral vertebra
LB73.28 - - - - - Sacrum agenesis or hypoplasia
LB73.29 - - - - - Caudal appendage
LB73.2A - - - - - Congenital spondylolisthesis
LB73.2Y - - - - - Other specified structural developmental anomalies of spine
LB73.2Z - - - - - Structural developmental anomalies of spine, unspecified
LB73.Y - - - - Other specified structural developmental anomalies of spine or bony thorax
LB73.Z - - - - Structural developmental anomalies of spine or bony thorax, unspecified
LB74 - - - Structural developmental anomalies of pelvic girdle
LB74.0 - - - - Developmental dysplasia of hip
LB74.1 - - - - Congenital subluxation of hip
LB74.2 - - - - Unstable hip
LB74.3 - - - - Congenital coxa vara
LB74.4 - - - - Congenital coxa valga
LB74.5 - - - - Wide symphysis pubis
LB74.Y - - - - Other specified structural developmental anomalies of pelvic girdle
LB74.Z - - - - Structural developmental anomalies of pelvic girdle, unspecified
LB75 - - - Brachydactyly
LB75.0 - - - - Brachydactyly of fingers
LB75.1 - - - - Brachydactyly of toes
LB75.2 - - - - Symbrachydactyly of hands or feet
LB75.Y - - - - Other specified brachydactyly
LB75.Z - - - - Brachydactyly, unspecified
LB76 - - - Triphalangeal thumb
LB77 - - - Hyperphalangy
LB78 - - - Polydactyly
LB78.0 - - - - Polydactyly of the thumb
LB78.1 - - - - Polysyndactyly
LB78.2 - - - - Postaxial polydactyly of fingers
LB78.3 - - - - Polydactyly of toes
LB78.Y - - - - Other specified polydactyly
LB78.Z - - - - Polydactyly, unspecified
LB79 - - - Syndactyly
LB79.0 - - - - Fused fingers
LB79.1 - - - - Webbed fingers
LB79.2 - - - - Fused toes
LB79.3 - - - - Webbed toes
LB79.Y - - - - Other specified syndactyly
LB79.Z - - - - Syndactyly, unspecified
- - - Congenital deformities of fingers or toes
LB80 - - - - Congenital deformities of fingers
LB80.0 - - - - - Clinodactyly of fingers
LB80.1 - - - - - Congenital club finger
LB80.2 - - - - - Radial deviation of fingers
LB80.Y - - - - - Other specified congenital deformities of fingers
LB81 - - - - Congenital deformities of toes
LB81.0 - - - - - Clinodactyly of toes
LB81.Y - - - - - Other specified congenital deformities of toes
LB8Z - - - - Congenital deformities of fingers or toes, unspecified
LB90 - - - Joint formation defects
LB90.0 - - - - Humero-radio-ulnar synostosis
LB90.1 - - - - Humero-radial synostosis
LB90.2 - - - - Humero-ulnar synostosis
LB90.3 - - - - Radio-ulnar synostosis
LB90.4 - - - - Madelung deformity
LB90.5 - - - - Congenital digital clubbing
LB90.6 - - - - Tibio-fibular synostosis
LB90.7 - - - - Cubitus valgus
LB90.8 - - - - Cubitus varus
LB90.Y - - - - Other specified joint formation defects
LB90.Z - - - - Joint formation defects, unspecified
LB91 - - - Congenital shoulder dislocation
LB92 - - - Congenital elbow dislocation
LB93 - - - Congenital knee dislocation
LB93.0 - - - - Congenital genu recurvatum
LB93.1 - - - - Congenital genu flexum
LB93.Y - - - - Other specified congenital knee dislocation
LB93.Z - - - - Congenital knee dislocation, unspecified
LB94 - - - Congenital patella dislocation
LB95 - - - Patella aplasia or hypoplasia
LB96 - - - Congenital bowing of long bones
LB96.0 - - - - Congenital bowing of femur
LB96.1 - - - - Congenital bowing of tibia
LB96.Y - - - - Other specified congenital bowing of long bones
LB96.Z - - - - Congenital bowing of long bones, unspecified
LB97 - - - Limb overgrowth
LB97.0 - - - - Macrodactyly of fingers
LB97.1 - - - - Macrodactyly of toes
LB97.2 - - - - Upper limb hypertrophy
LB97.3 - - - - Lower limb hypertrophy
LB97.Y - - - - Other specified limb overgrowth
LB97.Z - - - - Limb overgrowth, unspecified
LB98 - - - Congenital deformities of feet
LB98.0 - - - - Congenital varus deformities of feet
LB98.00 - - - - - Talipes equinovarus
LB98.01 - - - - - Talipes calcaneovarus
LB98.02 - - - - - Metatarsus varus
LB98.0Y - - - - - Other specified congenital varus deformities of feet
LB98.0Z - - - - - Congenital varus deformities of feet, unspecified
LB98.1 - - - - Congenital pes planus
LB98.2 - - - - Congenital valgus deformities of feet
LB98.20 - - - - - Congenital hallux valgus
LB98.21 - - - - - Metatarsus valgus
LB98.22 - - - - - Talipes calcaneovalgus
LB98.2Y - - - - - Other specified congenital valgus deformities of feet
LB98.2Z - - - - - Congenital valgus deformities of feet, unspecified
LB98.3 - - - - Congenital pes cavus
LB98.4 - - - - Congenital vertical talus
LB98.5 - - - - Congenital hammer toe
LB98.Y - - - - Other specified congenital deformities of feet
LB98.Z - - - - Congenital deformities of feet, unspecified
LB99 - - - Reduction defects of upper limb
LB99.0 - - - - Amelia of upper limb
LB99.1 - - - - Humeral agenesis or hypoplasia
LB99.2 - - - - Radial hemimelia
LB99.3 - - - - Ulnar hemimelia
LB99.4 - - - - Congenital absence of upper arm or forearm with hand present
LB99.5 - - - - Congenital absence of both forearm and hand
LB99.6 - - - - Acheiria
LB99.7 - - - - Adactyly of hands
LB99.8 - - - - Split hand
LB99.Y - - - - Other specified reduction defects of upper limb
LB99.Z - - - - Reduction defects of upper limb, unspecified
LB9A - - - Reduction defects of lower limb
LB9A.0 - - - - Amelia of lower limb
LB9A.1 - - - - Tibial hemimelia
LB9A.2 - - - - Fibular hemimelia
LB9A.3 - - - - Congenital absence of thigh or lower leg with foot present
LB9A.4 - - - - Apodia
LB9A.5 - - - - Adactyly of feet
LB9A.6 - - - - Split foot
LB9A.7 - - - - Congenital absence of both lower leg and foot
LB9A.8 - - - - Femoral agenesis or hypoplasia
LB9A.Y - - - - Other specified reduction defects of lower limb
LB9A.Z - - - - Reduction defects of lower limb, unspecified
LB9B - - - Reduction defects of upper or lower limbs
LB9Y - - - Other specified structural developmental anomalies of the skeleton
LB9Z - - - Structural developmental anomalies of the skeleton, unspecified
- - Structural developmental anomalies of the skin
- - - Developmental hamartomata of the epidermis and epidermal appendages
LC00 - - - - Keratinocytic epidermal hamartoma
LC00.0 - - - - - Epidermal naevus
LC00.Y - - - - - Other specified keratinocytic epidermal hamartoma
LC01 - - - - Pilosebaceous hamartoma
LC02 - - - - Complex epidermal hamartoma
LC0Y - - - - Other specified developmental hamartomata of the epidermis and epidermal appendages
- - - Developmental anomalies of skin pigmentation
LC10 - - - - Dermal melanocytosis
LC1Y - - - - Other specified developmental anomalies of skin pigmentation
- - - Hamartomata derived from dermal connective tissue
LC20 - - - - Connective tissue hamartoma
LC2Y - - - - Other specified hamartomata derived from dermal connective tissue
- - - Developmental defects of hair or nails
LC30 - - - - Developmental defects of hair or hair growth
LC31 - - - - Developmental defects of the nail apparatus
LC40 - - - Dermoid cyst
- - - Developmental anomalies of cutaneous vasculature
LC50 - - - - Developmental capillary vascular malformations of the skin
LC50.0 - - - - - Salmon patch
LC50.1 - - - - - Port-wine stain
LC50.Y - - - - - Other specified cutaneous capillary vascular malformation
LC51 - - - - Developmental venous malformations involving the skin
LC52 - - - - Complex or combined developmental vascular malformations involving the skin
LC5Y - - - - Other specified developmental anomalies of cutaneous vasculature
LC5Z - - - - Cutaneous vascular malformation, unspecified
- - - Congenital anomalies of skin development
LC60 - - - - Aplasia cutis congenita
LC7Y - - - Other specified structural developmental anomalies of the skin
LC7Z - - - Structural developmental anomalies of the skin, unspecified
- - Structural developmental anomalies of the adrenal glands
LC80 - - - Congenital adrenal hypoplasia
LC8Y - - - Other specified structural developmental anomalies of the adrenal glands
LC8Z - - - Structural developmental anomalies of the adrenal glands, unspecified
LD0Y - - Other specified structural developmental anomalies primarily affecting one body system
LD0Z - - Structural developmental anomalies primarily affecting one body system, unspecified
- Multiple developmental anomalies or syndromes
LD20 - - Syndromes with central nervous system anomalies as a major feature
LD20.0 - - - Syndromes with cerebellar anomalies as a major feature
LD20.00 - - - - Joubert syndrome
LD20.01 - - - - Pontocerebellar hypoplasia
LD20.0Y - - - - Other specified syndromes with cerebellar anomalies as a major feature
LD20.0Z - - - - Syndromes with cerebellar anomalies as a major feature, unspecified
LD20.1 - - - Syndromes with lissencephaly as a major feature
LD20.2 - - - Syndromes with microcephaly as a major feature
LD20.3 - - - Syndromes with holoprosencephaly as a major feature
LD20.4 - - - Brain calcifications
LD20.Y - - - Other specified syndromes with central nervous system anomalies as a major feature
LD20.Z - - - Syndromes with central nervous system anomalies as a major feature, unspecified
LD21 - - Syndromes with eye anomalies as a major feature
LD21.0 - - - Syndromes with microphthalmia as a major feature
LD21.Y - - - Other specified syndromes with eye anomalies as a major feature
LD21.Z - - - Syndromes with eye anomalies as a major feature, unspecified
LD22 - - Syndromes with dental anomalies as a major feature
LD23 - - Syndromes with vascular anomalies as a major feature
LD24 - - Syndromes with skeletal anomalies as a major feature
LD24.0 - - - Syndromes with micromelia
LD24.00 - - - - Achondroplasia
LD24.01 - - - - Hypochondroplasia
LD24.02 - - - - Thanatophoric dysplasia
LD24.03 - - - - Diastrophic dysplasia
LD24.04 - - - - Chondrodysplasia punctata
LD24.0Y - - - - Other specified syndromes with micromelia
LD24.0Z - - - - Syndromes with micromelia, unspecified
LD24.1 - - - Bone diseases with increased bone density
LD24.10 - - - - Osteopetrosis
LD24.11 - - - - Osteopoikilosis
LD24.1Y - - - - Other specified bone diseases with increased bone density
LD24.1Z - - - - Bone diseases with increased bone density, unspecified
LD24.2 - - - Bone diseases with disorganised development of skeletal components
LD24.20 - - - - Multiple osteochondromas
LD24.21 - - - - Exostoses with anetodermia and brachydactyly type E
LD24.22 - - - - Cherubism
LD24.23 - - - - Yunis-Varon disease
LD24.2Y - - - - Other specified bone diseases with disorganised development of skeletal components
LD24.2Z - - - - Bone diseases with disorganised development of skeletal components, unspecified
LD24.3 - - - Spondyloepiphyseal or spondyloepimetaphyseal dysplasias
LD24.4 - - - Spondylometaphyseal dysplasias
LD24.5 - - - Spondylodysplastic dysplasias
LD24.50 - - - - Achondrogenesis
LD24.51 - - - - Hypochondrogenesis
LD24.5Y - - - - Other specified spondylodysplastic dysplasias
LD24.5Z - - - - Spondylodysplastic dysplasias, unspecified
LD24.6 - - - Multiple epiphyseal dysplasia or pseudoachondroplasia
LD24.60 - - - - Pseudoachondroplasia
LD24.61 - - - - Multiple epiphyseal dysplasias
LD24.6Y - - - - Other specified multiple epiphyseal dysplasia or pseudoachondroplasia
LD24.6Z - - - - Multiple epiphyseal dysplasia or pseudoachondroplasia, unspecified
LD24.7 - - - Multiple metaphyseal dysplasias
LD24.8 - - - Acromelic dysplasias
LD24.80 - - - - Langer-Giedion syndrome
LD24.8Y - - - - Other specified acromelic dysplasias
LD24.8Z - - - - Acromelic dysplasias, unspecified
LD24.9 - - - Acromesomelic dysplasias
LD24.A - - - Mesomelic or rhizomesomelic dysplasias
LD24.B - - - Short rib syndromes
LD24.B0 - - - - Short rib-polydactyly syndrome
LD24.B1 - - - - Asphyxiating thoracic dystrophy
LD24.BY - - - - Other specified short rib syndromes
LD24.BZ - - - - Short rib syndromes, unspecified
LD24.C - - - Bent bone dysplasias
LD24.D - - - Slender bone dysplasias
LD24.E - - - Bone dysplasias with multiple joint dislocations
LD24.F - - - Progressive ossification of skin, skeletal muscle, fascia, tendons or ligaments
LD24.G - - - Syndromic craniosynostoses
LD24.G0 - - - - Pfeiffer syndrome
LD24.G1 - - - - Crouzon disease
LD24.G2 - - - - Apert syndrome
LD24.GY - - - - Other specified syndromic craniosynostoses
LD24.GZ - - - - Syndromic craniosynostoses, unspecified
LD24.H - - - Dysostoses with predominant vertebral and costal involvement
LD24.J - - - Patellar dysostoses
LD24.J0 - - - - Nail-patella syndrome
LD24.JY - - - - Other specified patellar dysostoses
LD24.JZ - - - - Patellar dysostoses, unspecified
LD24.K - - - Genetic bone diseases with decreased bone density
LD24.K0 - - - - Osteogenesis imperfecta
LD24.KY - - - - Other specified genetic bone diseases with decreased bone density
LD24.KZ - - - - Genetic bone diseases with decreased bone density, unspecified
LD24.Y - - - Other specified syndromes with skeletal anomalies as a major feature
LD24.Z - - - Syndromes with skeletal anomalies as a major feature, unspecified
LD25 - - Syndromes with face or limb anomalies as a major feature
LD25.0 - - - Oromandibular-limb anomaly syndrome
LD25.00 - - - - Oral-facial-digital syndrome
LD25.0Y - - - - Other specified oromandibular-limb anomaly syndrome
LD25.0Z - - - - Oromandibular-limb anomaly syndrome, unspecified
LD25.1 - - - Fronto-otopalatodigital syndromes
LD25.2 - - - Acrofacial dysostoses
LD25.3 - - - Craniofacial dysostoses
LD25.Y - - - Other specified syndromes with face or limb anomalies as a major feature
LD25.Z - - - Syndromes with face or limb anomalies as a major feature, unspecified
LD26 - - Syndromes with limb anomalies as a major feature
LD26.0 - - - Combined reduction defects of upper and lower limbs
LD26.1 - - - Complex brachydactylies
LD26.2 - - - Syndromes with limb duplication, polydactyly, syndactyly or triphalangism
LD26.3 - - - Syndromes with synostoses of limbs
LD26.4 - - - Arthrogryposis syndromes
LD26.40 - - - - Multiple pterygium syndrome
LD26.41 - - - - Arthrogryposis multiplex congenita
LD26.4Y - - - - Other specified arthrogryposis syndromes
LD26.4Z - - - - Arthrogryposis syndromes, unspecified
LD26.5 - - - Constriction rings
LD26.6 - - - Congenital vascular bone syndromes
LD26.60 - - - - Angio-osteohypertrophic syndrome
LD26.6Y - - - - Other specified congenital vascular bone syndromes
LD26.6Z - - - - Congenital vascular bone syndromes, unspecified
LD26.Y - - - Other specified syndromes with limb anomalies as a major feature
LD26.Z - - - Syndromes with limb anomalies as a major feature, unspecified
LD27 - - Syndromes with skin or mucosal anomalies as a major feature
LD27.0 - - - Ectodermal dysplasia syndromes
LD27.00 - - - - Incontinentia pigmenti
LD27.01 - - - - Cronkhite-Canada syndrome
LD27.02 - - - - Hypohidrotic ectodermal dysplasia
LD27.03 - - - - Hidrotic ectodermal dysplasia, Clouston type
LD27.0Y - - - - Other specified ectodermal dysplasia syndromes
LD27.1 - - - Xeroderma pigmentosum
LD27.2 - - - Syndromic ichthyosis
LD27.3 - - - Genetic syndromes with hypertrichosis
LD27.4 - - - Genetic syndromes affecting nails
LD27.5 - - - Genetic hamartoneoplastic syndromes affecting the skin
LD27.6 - - - Genetic lipodystrophy
LD27.60 - - - - Congenital generalised lipodystrophy
LD27.6Z - - - - Genetic lipodystrophy, unspecified
LD27.Y - - - Other specified syndromes with skin or mucosal anomalies as a major feature
LD27.Z - - - Syndromes with skin or mucosal anomalies as a major feature, unspecified
LD28 - - Syndromes with connective tissue involvement as a major feature
LD28.0 - - - Marfan syndrome or Marfan-related disorders
LD28.00 - - - - Congenital contractural arachnodactyly
LD28.01 - - - - Marfan syndrome
LD28.0Y - - - - Other specified Marfan syndrome or Marfan-related disorders
LD28.0Z - - - - Marfan syndrome or Marfan-related disorders, unspecified
LD28.1 - - - Ehlers-Danlos syndrome
LD28.10 - - - - Ehlers-Danlos syndrome, classical type
LD28.1Y - - - - Other specified types of Ehlers-Danlos syndrome
LD28.2 - - - Genetically-determined cutis laxa
LD28.Y - - - Other specified syndromes with connective tissue involvement as a major feature
LD28.Z - - - Syndromes with connective tissue involvement as a major feature, unspecified
LD29 - - Syndromes with obesity as a major feature
LD2A - - Malformative disorders of sex development
LD2A.0 - - - Ovotesticular disorder of sex development
LD2A.1 - - - 46,XY gonadal dysgenesis
LD2A.2 - - - Testicular agenesis
LD2A.3 - - - 46,XY disorder of sex development due to a defect in testosterone metabolism
LD2A.4 - - - 46,XY disorder of sex development due to androgen resistance
LD2A.Y - - - Other specified malformative disorders of sex development
LD2A.Z - - - Malformative disorders of sex development, unspecified
LD2B - - Syndromes with premature ageing appearance as a major feature
LD2C - - Overgrowth syndromes
LD2D - - Phakomatoses or hamartoneoplastic syndromes
LD2D.0 - - - Peutz-Jeghers syndrome
LD2D.1 - - - Neurofibromatoses
LD2D.10 - - - - Neurofibromatosis type 1
LD2D.11 - - - - Neurofibromatosis type 2
LD2D.12 - - - - Neurofibromatosis type 3
LD2D.1Y - - - - Other specified neurofibromatoses
LD2D.1Z - - - - Neurofibromatosis, unspecified
LD2D.2 - - - Tuberous sclerosis
LD2D.3 - - - Gardner syndrome
LD2D.4 - - - Gorlin syndrome
LD2D.Y - - - Other specified phakomatoses or hamartoneoplastic syndromes
LD2D.Z - - - Phakomatoses or hamartoneoplastic syndromes, unspecified
LD2E - - Syndromes with structural anomalies due to inborn errors of metabolism
LD2F - - Syndromes with multiple structural anomalies, without predominant body system involvement
LD2F.0 - - - Toxic or drug-related embryofetopathies
LD2F.00 - - - - Foetal alcohol syndrome
LD2F.01 - - - - Foetal hydantoin syndrome
LD2F.02 - - - - Embryofetopathy due to oral anticoagulant therapy
LD2F.0Y - - - - Other specified toxic or drug-related embryofetopathies
LD2F.0Z - - - - Toxic or drug-related embryofetopathies, unspecified
LD2F.1 - - - Syndromes with multiple structural anomalies, not of environmental origin
LD2F.10 - - - - Prune belly syndrome
LD2F.11 - - - - VATER association
LD2F.12 - - - - Sirenomelia
LD2F.13 - - - - Meckel-Gruber syndrome
LD2F.14 - - - - MURCS association
LD2F.15 - - - - Noonan syndrome
LD2F.16 - - - - Otomandibular dysplasia
LD2F.1Y - - - - Other specified syndromes with multiple structural anomalies, not of environmental origin
LD2F.1Z - - - - Syndromes with multiple structural anomalies, not of environmental origin, unspecified
LD2F.Y - - - Other specified syndromes with multiple structural anomalies, without predominant body system involvement
LD2F.Z - - - Syndromes with multiple structural anomalies, without predominant body system involvement, unspecified
LD2G - - Conjoined twins
LD2H - - Syndromic genetic deafness
LD2H.0 - - - Fraser syndrome
LD2H.1 - - - Neuropathy with hearing impairment
LD2H.2 - - - Progressive deafness with stapes fixation
LD2H.3 - - - Waardenburg-Shah syndrome
LD2H.4 - - - Usher syndrome
LD2H.Y - - - Other specified syndromic genetic deafness
LD2H.Z - - - Syndromic genetic deafness, unspecified
LD2Y - - Other specified multiple developmental anomalies or syndromes
LD2Z - - Multiple developmental anomalies or syndromes, unspecified
- Chromosomal anomalies, excluding gene mutations
LD40 - - Complete trisomies of the autosomes
LD40.0 - - - Complete trisomy 21
LD40.1 - - - Complete trisomy 13
LD40.2 - - - Complete trisomy 18
LD40.Y - - - Other specified complete trisomies of the autosomes
LD40.Z - - - Complete trisomies of the autosomes, unspecified
LD41 - - Duplications of the autosomes
LD41.0 - - - Duplications of chromosome 1
LD41.00 - - - - Duplications of the long arm of chromosome 1
LD41.01 - - - - Duplications of the short arm of chromosome 1
LD41.0Y - - - - Other specified duplications of chromosome 1
LD41.0Z - - - - Duplications of chromosome 1, unspecified
LD41.1 - - - Duplications of chromosome 2
LD41.10 - - - - Duplications of the long arm of chromosome 2
LD41.11 - - - - Duplications of the short arm of chromosome 2
LD41.1Y - - - - Other specified duplications of chromosome 2
LD41.1Z - - - - Duplications of chromosome 2, unspecified
LD41.2 - - - Duplications of chromosome 3
LD41.20 - - - - Duplications of the long arm of chromosome 3
LD41.21 - - - - Duplications of the short arm of chromosome 3
LD41.2Y - - - - Other specified duplications of chromosome 3
LD41.2Z - - - - Duplications of chromosome 3, unspecified
LD41.3 - - - Duplications of chromosome 4
LD41.30 - - - - Duplications of the long arm of chromosome 4
LD41.31 - - - - Duplications of the short arm of chromosome 4
LD41.3Y - - - - Other specified duplications of chromosome 4
LD41.3Z - - - - Duplications of chromosome 4, unspecified
LD41.4 - - - Duplications of chromosome 5
LD41.40 - - - - Duplications of the long arm of chromosome 5
LD41.41 - - - - Duplications of the short arm of chromosome 5
LD41.4Y - - - - Other specified duplications of chromosome 5
LD41.4Z - - - - Duplications of chromosome 5, unspecified
LD41.5 - - - Duplications of chromosome 6
LD41.50 - - - - Duplications of the long arm of chromosome 6
LD41.51 - - - - Duplications of the short arm of chromosome 6
LD41.5Y - - - - Other specified duplications of chromosome 6
LD41.5Z - - - - Duplications of chromosome 6, unspecified
LD41.6 - - - Duplications of chromosome 7
LD41.60 - - - - Duplications of the long arm of chromosome 7
LD41.61 - - - - Duplications of the short arm of chromosome 7
LD41.6Y - - - - Other specified duplications of chromosome 7
LD41.6Z - - - - Duplications of chromosome 7, unspecified
LD41.7 - - - Duplications of chromosome 8
LD41.70 - - - - Duplications of the long arm of chromosome 8
LD41.71 - - - - Duplications of the short arm of chromosome 8
LD41.7Y - - - - Other specified duplications of chromosome 8
LD41.7Z - - - - Duplications of chromosome 8, unspecified
LD41.8 - - - Duplications of chromosome 9
LD41.80 - - - - Duplications of the long arm of chromosome 9
LD41.81 - - - - Duplications of the short arm of chromosome 9
LD41.8Y - - - - Other specified duplications of chromosome 9
LD41.8Z - - - - Duplications of chromosome 9, unspecified
LD41.9 - - - Duplications of chromosome 10
LD41.90 - - - - Duplications of the long arm of chromosome 10
LD41.91 - - - - Duplications of the short arm of chromosome 10
LD41.9Y - - - - Other specified duplications of chromosome 10
LD41.9Z - - - - Duplications of chromosome 10, unspecified
LD41.A - - - Duplications of chromosome 11
LD41.B - - - Duplications of chromosome 12
LD41.B0 - - - - Duplications of the long arm of chromosome 12
LD41.B1 - - - - Duplications of the short arm of chromosome 12
LD41.BY - - - - Other specified duplications of chromosome 12
LD41.BZ - - - - Duplications of chromosome 12, unspecified
LD41.C - - - Duplications of chromosome 13
LD41.D - - - Duplications of chromosome 14
LD41.E - - - Duplications of chromosome 15
LD41.F - - - Duplications of chromosome 16
LD41.F0 - - - - Duplications of the long arm of chromosome 16
LD41.F1 - - - - Duplications of the short arm of chromosome 16
LD41.FY - - - - Other specified duplications of chromosome 16
LD41.FZ - - - - Duplications of chromosome 16, unspecified
LD41.G - - - Duplications of chromosome 17
LD41.G0 - - - - Duplications of the long arm of chromosome 17
LD41.G1 - - - - Duplications of the short arm of chromosome 17
LD41.GY - - - - Other specified duplications of chromosome 17
LD41.GZ - - - - Duplications of chromosome 17, unspecified
LD41.H - - - Duplications of chromosome 18
LD41.H0 - - - - Duplications of the long arm of chromosome 18
LD41.H1 - - - - Duplications of the short arm of chromosome 18
LD41.HY - - - - Other specified duplications of chromosome 18
LD41.HZ - - - - Duplications of chromosome 18, unspecified
LD41.J - - - Duplications of chromosome 19
LD41.J0 - - - - Duplications of the long arm of chromosome 19
LD41.J1 - - - - Duplications of the short arm of chromosome 19
LD41.JY - - - - Other specified duplications of chromosome 19
LD41.JZ - - - - Duplications of chromosome 19, unspecified
LD41.K - - - Duplications of chromosome 20
LD41.K0 - - - - Duplications of the long arm of chromosome 20
LD41.K1 - - - - Duplications of the short arm of chromosome 20
LD41.KY - - - - Other specified duplications of chromosome 20
LD41.KZ - - - - Duplications of chromosome 20, unspecified
LD41.L - - - Duplications of chromosome 21
LD41.M - - - Duplications of chromosome 22
LD41.N - - - Extra ring or dicentric chromosomes
LD41.P - - - Duplications with other complex rearrangements
LD41.Q - - - Extra marker chromosomes
LD41.Y - - - Other specified duplications of the autosomes
LD41.Z - - - Duplications of the autosomes, unspecified
LD42 - - Polyploidies
LD42.0 - - - Triploidy
LD42.1 - - - Tetraploidy
LD42.Y - - - Other specified polyploidies
LD42.Z - - - Polyploidies, unspecified
LD43 - - Complete monosomies of the autosomes
LD43.0 - - - Complete monosomy of autosome
LD43.1 - - - Mosaic monosomy of autosome
LD43.Y - - - Other specified complete monosomies of the autosomes
LD43.Z - - - Complete monosomies of the autosomes, unspecified
LD44 - - Deletions of the autosomes
LD44.0 - - - Chromosome replaced with ring or dicentric with normal number of chromosomes
LD44.1 - - - Deletions of chromosome 1
LD44.10 - - - - Deletions of the long arm of chromosome 1
LD44.11 - - - - Deletions of the short arm of chromosome 1
LD44.1Y - - - - Other specified deletions of chromosome 1
LD44.1Z - - - - Deletions of chromosome 1, unspecified
LD44.2 - - - Deletions of chromosome 2
LD44.20 - - - - Deletions of the long arm of chromosome 2
LD44.21 - - - - Deletions of the short arm of chromosome 2
LD44.2Y - - - - Other specified deletions of chromosome 2
LD44.2Z - - - - Deletions of chromosome 2, unspecified
LD44.3 - - - Deletions of chromosome 3
LD44.30 - - - - Deletions of the long arm of chromosome 3
LD44.31 - - - - Deletions of the short arm of chromosome 3
LD44.3Y - - - - Other specified deletions of chromosome 3
LD44.3Z - - - - Deletions of chromosome 3, unspecified
LD44.4 - - - Deletions of chromosome 4
LD44.40 - - - - Deletions of the long arm of chromosome 4
LD44.41 - - - - Deletions of the short arm of chromosome 4
LD44.4Y - - - - Other specified deletions of chromosome 4
LD44.4Z - - - - Deletions of chromosome 4, unspecified
LD44.5 - - - Deletions of chromosome 5
LD44.50 - - - - Deletions of the long arm of chromosome 5
LD44.51 - - - - Deletions of the short arm of chromosome 5
LD44.5Y - - - - Other specified deletions of chromosome 5
LD44.5Z - - - - Deletions of chromosome 5, unspecified
LD44.6 - - - Deletions of chromosome 6
LD44.60 - - - - Deletions of the long arm of chromosome 6
LD44.61 - - - - Deletions of the short arm of chromosome 6
LD44.6Y - - - - Other specified deletions of chromosome 6
LD44.6Z - - - - Deletions of chromosome 6, unspecified
LD44.7 - - - Deletions of chromosome 7
LD44.70 - - - - Deletions of the long arm of chromosome 7
LD44.71 - - - - Deletions of the short arm of chromosome 7
LD44.7Y - - - - Other specified deletions of chromosome 7
LD44.7Z - - - - Deletions of chromosome 7, unspecified
LD44.8 - - - Deletions of chromosome 8
LD44.80 - - - - Deletions of the long arm of chromosome 8
LD44.81 - - - - Deletions of the short arm of chromosome 8
LD44.8Y - - - - Other specified deletions of chromosome 8
LD44.8Z - - - - Deletions of chromosome 8, unspecified
LD44.9 - - - Deletions of chromosome 9
LD44.90 - - - - Deletions of the long arm of chromosome 9
LD44.91 - - - - Deletions of the short arm of chromosome 9
LD44.9Y - - - - Other specified deletions of chromosome 9
LD44.9Z - - - - Deletions of chromosome 9, unspecified
LD44.A - - - Deletions of chromosome 10
LD44.A0 - - - - Deletions of the long arm of chromosome 10
LD44.A1 - - - - Deletions of the short arm of chromosome 10
LD44.AY - - - - Other specified deletions of chromosome 10
LD44.AZ - - - - Deletions of chromosome 10, unspecified
LD44.B - - - Deletions of chromosome 11
LD44.B0 - - - - Deletions of the long arm of chromosome 11
LD44.B1 - - - - Deletions of the short arm of chromosome 11
LD44.BY - - - - Other specified deletions of chromosome 11
LD44.BZ - - - - Deletions of chromosome 11, unspecified
LD44.C - - - Deletions of chromosome 12
LD44.C0 - - - - Deletions of the long arm of chromosome 12
LD44.C1 - - - - Deletions of the short arm of chromosome 12
LD44.CY - - - - Other specified deletions of chromosome 12
LD44.CZ - - - - Deletions of chromosome 12, unspecified
LD44.D - - - Deletions of chromosome 13
LD44.E - - - Deletions of chromosome 14
LD44.F - - - Deletions of chromosome 15
LD44.G - - - Deletions of chromosome 16
LD44.G0 - - - - Deletions of the long arm of chromosome 16
LD44.G1 - - - - Deletions of the short arm of chromosome 16
LD44.GY - - - - Other specified deletions of chromosome 16
LD44.GZ - - - - Deletions of chromosome 16, unspecified
LD44.H - - - Deletions of chromosome 17
LD44.H0 - - - - Deletions of the long arm of chromosome 17
LD44.H1 - - - - Deletions of the short arm of chromosome 17
LD44.HY - - - - Other specified deletions of chromosome 17
LD44.HZ - - - - Deletions of chromosome 17, unspecified
LD44.J - - - Deletions of chromosome 18
LD44.J0 - - - - Deletions of the long arm of chromosome 18
LD44.J1 - - - - Deletions of the short arm of chromosome 18
LD44.JY - - - - Other specified deletions of chromosome 18
LD44.JZ - - - - Deletions of chromosome 18, unspecified
LD44.K - - - Deletions of chromosome 19
LD44.K0 - - - - Deletions of the long arm of chromosome 19
LD44.K1 - - - - Deletions of the short arm of chromosome 19
LD44.KY - - - - Other specified deletions of chromosome 19
LD44.KZ - - - - Deletions of chromosome 19, unspecified
LD44.L - - - Deletions of chromosome 20
LD44.L0 - - - - Deletions of the long arm of chromosome 20
LD44.L1 - - - - Deletions of the short arm of chromosome 20
LD44.LY - - - - Other specified deletions of chromosome 20
LD44.LZ - - - - Deletions of chromosome 20, unspecified
LD44.M - - - Deletions of chromosome 21
LD44.N - - - Deletions of chromosome 22
LD44.N0 - - - - CATCH 22 phenotype
LD44.NY - - - - Other specified deletions of chromosome 22
LD44.NZ - - - - Deletions of chromosome 22, unspecified
LD44.P - - - Deletions with other complex rearrangements
LD44.Y - - - Other specified deletions of the autosomes
LD44.Z - - - Deletions of the autosomes, unspecified
LD45 - - Uniparental disomies
LD45.0 - - - Uniparental disomies of maternal origin
LD45.1 - - - Uniparental disomies of paternal origin
LD45.Y - - - Other specified uniparental disomies
LD45.Z - - - Uniparental disomies, unspecified
LD46 - - Imprinting errors
LD46.0 - - - Maternal imprinting error
LD46.1 - - - Paternal imprinting error
LD46.Y - - - Other specified imprinting errors
LD46.Z - - - Imprinting errors, unspecified
LD47 - - Balanced rearrangements or structural markers
LD47.0 - - - Balanced translocation and insertion in normal individual
LD47.1 - - - Chromosome inversion in normal individual
LD47.2 - - - Balanced autosomal rearrangement in abnormal individual
LD47.3 - - - Balanced sex or autosomal rearrangement in abnormal individual
LD47.4 - - - Autosomal fragile site
LD47.Y - - - Other specified balanced rearrangements or structural markers
LD47.Z - - - Balanced rearrangements or structural markers, unspecified
- - Sex chromosome anomalies
LD50 - - - Number anomalies of chromosome X
LD50.0 - - - - Turner syndrome
LD50.00 - - - - - Karyotype 45, X
LD50.01 - - - - - Karyotype 46, X iso Xq
LD50.02 - - - - - Karyotype 46, X with abnormal sex chromosome, except iso Xq
LD50.03 - - - - - Mosaicism, 45, X, 46, XX or XY
LD50.04 - - - - - Mosaicism, 45, X or other cell line with abnormal sex chromosome
LD50.1 - - - - Karyotype 47,XXX
LD50.2 - - - - Mosaicism, lines with various numbers of X chromosomes
LD50.3 - - - - Klinefelter syndrome
LD50.30 - - - - - Klinefelter syndrome with karyotype 47,XXY, regular
LD50.31 - - - - - Klinefelter syndrome, male with more than two X chromosomes
LD50.3Y - - - - - Other specified Klinefelter syndrome
LD50.Y - - - - Other specified number anomalies of chromosome X
LD50.Z - - - - Number anomalies of chromosome X, unspecified
LD51 - - - Structural anomalies of chromosome X, excluding Turner syndrome
LD52 - - - Number anomalies of chromosome Y
LD52.0 - - - - Male with 46,XX karyotype
LD52.1 - - - - Male with double or multiple Y
LD52.Y - - - - Other specified number anomalies of chromosome Y
LD52.Z - - - - Number anomalies of chromosome Y, unspecified
LD53 - - - Structural anomalies of chromosome Y
LD54 - - - Male with sex chromosome mosaicism
LD55 - - - Fragile X chromosome
LD56 - - - Chimaera 46, XX, 46, XY
LD56.0 - - - - Androgenetic chimaera
LD56.1 - - - - Gynogenetic chimaera
LD56.Y - - - - Other specified chimaera 46, XX, 46, XY
LD56.Z - - - - Chimaera 46, XX, 46, XY, unspecified
LD5Y - - - Other specified sex chromosome anomalies
LD5Z - - - Sex chromosome anomalies, unspecified
LD7Y - - Other specified chromosomal anomalies, excluding gene mutations
LD7Z - - Chromosomal anomalies, excluding gene mutations, unspecified
LD90 - Conditions with disorders of intellectual development as a relevant clinical feature
LD90.0 - - Angelman syndrome
LD90.1 - - Early-onset parkinsonism - intellectual deficit
LD90.2 - - Pelizaeus-Merzbacher-like disease
LD90.3 - - Prader-Willi syndrome
LD90.4 - - Rett syndrome
LD90.Y - - Other specified conditions with disorders of intellectual development as a relevant clinical feature
LD90.Z - - Conditions with disorders of intellectual development as a relevant clinical feature, unspecified
LD9Y - Other specified developmental anomalies
LD9Z - Developmental anomalies, unspecified

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Contributors: Prab R. Tumpati, MD