Category:Congenital disorders
From WikiMD's Wellness Encyclopedia
 | This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes Q00-Q99 should be included in this category. |
In medicine, a congenital disorder is a disorder that is present at birth.
Subcategories
This category has the following 7 subcategories, out of 7 total.
A
C
E
I
Pages in category "Congenital disorders"
The following 200 pages are in this category, out of 1,083 total.
(previous page) (next page)A
- A3P5PS
- Aagenaes syndrome
- ABCC7
- Abdominal defects
- Abdominal wall defects
- Ablepharon
- Abnormity
- Absence
- Absence deformity of leg-cataract syndrome
- Absent adrenal gland
- Absent body parts
- Acalvaria
- Acardiac twin
- Accessory auricle
- Accessory breast
- Accessory nipples
- Accessory pathway
- Accessory spleen
- Accessory talus
- Acephaly
- Acheilia
- Acheiria
- Acheiropodia
- Achelia
- Achiria
- Achondrogenesis
- Acral dysostosis with facial and genital abnormalities
- Acrania
- Acro fronto facio nasal dysostosis
- Acrodysostosis
- Adams–Nance syndrome
- Adducted thumb syndrome
- Afibrinogenemia
- Aganglionic megacolon
- Aganglionosis, total intestinal
- Agenesis
- Agenesis of corpus callosum
- Agenesis of the vena cava
- Aglossia
- Agnathia
- Al Awadi Teebi Farag syndrome
- Alcohol and pregnancy
- Amastia
- Amazia
- Amc
- Amelia
- Amelia (birth defect)
- Amelia cleft lip palate hydrocephalus iris coloboma
- Amorphous globosus
- Amorphus
- Anemia, hypoplastic, congenital
- Anencephalus
- Ankyloblepharon
- Ankyloblepharon filiforme adnatum
- Anophthalmia esophageal atresia cryptorchidism
- Anophthalmia megalocornea cardiopathy skeletal anomalies syndrome
- Anophthalmos with limb anomalies
- Anorectal anomalies
- Anorectal atresia
- Anotia
- Anterior segment mesenchymal dysgenesis
- Aorta-pulmonary artery fistula
- Apical ectodermal ridge
- Aplasia cutis
- Aposthia
- Aprosencephaly cerebellar dysgenesis
- Aprosencephaly-atelencephaly syndrome
- Aprosopus
- Aqueductal stenosis
- Arachnoid cysts
- Intracranial cysts
- Arakawa's syndrome II
- Arcuate uterus
- Armless
- Arnold Chiari malformation
- Arnold-Chiari malformations
- Arteriovenous fistula
- Arthrogryposis ectodermal dysplasia other anomalies
- Arthrogryposis multiplex congenita, distal type 1
- Arthrogryposis multiplex congenita, distal type 2
- Asphyxiating thoracic dysplasia 3
- Asplenia with cardiovascular anomalies
- Asymmetric crying facies
- Ateliosis
- Athelia
- Atransferrinemia
- Atresia
- Atresia of small intestine
- Atretic
- Autopodium
- Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
B
- Bamforth-Lazarus syndrome
- Bamforth–Lazarus syndrome
- Barakat syndrome
- Bartter syndrome
- Bartter syndrome type 3
- Basilar impression primary
- Bd syndrome
- Beckwith Wiedemann syndrome
- Beckwith-wiedemann syndrome
- Benign congenital hypotonia
- Bidactyly
- Bifid
- Bifid nose dominant
- Bilateral optic nerve hypoplasia
- Biliary atresia, extrahepatic
- Biliary atresia, intrahepatic, syndromic form
- Biliary hamartomas
- Biliary hypoplasia
- Binder
- Bladder exstrophy
- Blepharophimosis ptosis syndactyly mental retardation
- Blepharophimosis, ptosis, epicanthus inversus
- Blepharoptosis
- Blue baby
- Bochdalek hernia
- Body stalk anomaly
- Bone deformity
- Bone dysplasia corpus callosum agenesis
- Bone malrotation
- Bonnet Dechaume Blanc syndrome
- Boomerang dysplasia
- Borrone Di Rocco Crovato syndrome
- Bosma arhinia microphthalmia syndrome
- Boudhina Yedes Khiari syndrome
- Bowen-Conradi syndrome
- Brachial amelia, cleft lip, and holoprosencephaly
- Brachycephaly deafness cataract mental retardation
- Brachydactyly
- Brachydactyly Ballard type
- Brachydactyly clinodactyly
- Brachydactyly Haws type
- Brachydactyly of the hands and feet with duplication of the first toes
- Brachydactyly Smorgasbord type
- Brachydactyly type A3
- Brachydactyly type A5
- Brachydactyly type A5 nail dysplasia
- Brachydactyly type A6
- Brachydactyly type A7
- Brachydactyly type D
- Brachydactyly with major proximal phalangeal shortening
- Brachygnathism
- Brachymesophalangy II and V
- Brachymetatarsia
- Brachyturricephaly
- Branchial arch defects
- Branchial cleft
- Branchial cleft cyst
- Branchial fistula
- Breast aplasia
- Breast hypoplasia
- Brown syndrome
- Brown's
- Buphthalmos
C
- Cacchi Ricci disease
- CAMFAK syndrome
- Camptodactyly
- Camptodactyly joint contractures facial skeletal dysplasia
- Camptodactyly overgrowth unusual facies
- Camptodactyly vertebral fusion
- Cantrell deformity
- Cantrell syndrome
- Cantú syndrome
- Cardiac valvular dysplasia, X-linked
- Cardiocranial syndrome, Pfeiffer type
- Cardiofacial syndrome short limbs
- Cardiogenetic disorders
- Cardiomelic syndrome Stratton Koehler type
- Carey Fineman Ziter syndrome
- Carnevale–Krajewska–Fischetto syndrome
- Caroli
- Cassia–Stocco–Dos Santos syndrome
- Cat eye syndrome
- Cataract, congenital ichthyosis
- Caudal duplication
- Caudal regression sequence
- Cayler cardiofacial syndrome
- CDH
- CDK13-related disorder
- Cebocephaly
- CELSR1
- Central core disease of muscle
- Central nervous system cavernous hemangioma
- Cephalopolysyndactyly
- Cerebellar hypoplasia
- Cerebral calcification cerebellar hypoplasia
- Cerebral palsy
- Cerebro facio thoracic dysplasia
- Cerebro reno digital syndrome
- Cervical agenesis
