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 983 total.
(previous page) (next page)A
- A3P5PS
- Aagenaes syndrome
- Aarskog syndrome
- ABCC7
- Abdominal defects
- Abdominal wall defects
- Ablepharon
- Abnormity
- Absence
- Absence deformity of leg-cataract syndrome
- Absent body parts
- Acalvaria
- Acardiac twin
- Accessory auricle
- Accessory breast
- Accessory nipples
- Accessory pathway
- Accessory spleen
- Accessory talus
- Acephaly
- Acheilia
- Acheiria
- Achelia
- Achiria
- Achondrogenesis
- Acrania
- Acrodysostosis
- Adams–Nance syndrome
- Afibrinogenemia
- Agenesis
- Agenesis of corpus callosum
- Agenesis of the vena cava
- Aglossia
- Agnathia
- Alcohol and pregnancy
- Amastia
- Amazia
- Amelia
- Amelia (birth defect)
- Amelia cleft lip palate hydrocephalus iris coloboma
- Amorphous globosus
- Amorphus
- Anemia, hypoplastic, congenital
- Ankyloblepharon
- Anophthalmia megalocornea cardiopathy skeletal anomalies syndrome
- Anorectal anomalies
- Anorectal atresia
- Anotia
- Anterior segment mesenchymal dysgenesis
- Apical ectodermal ridge
- Aplasia cutis
- Aposthia
- Aprosencephaly cerebellar dysgenesis
- Aprosopus
- Aqueductal stenosis
- Arachnoid cysts
- Intracranial cysts
- Arakawa's syndrome II
- Arcuate uterus
- Armless
- 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
- Atretic
- Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
B
- Bamforth–Lazarus syndrome
- Barakat syndrome
- Bartter syndrome
- Bartter syndrome type 3
- Basilar impression primary
- 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
- Bone deformity
- Bone dysplasia corpus callosum agenesis
- Bone malrotation
- Bonnet Dechaume Blanc syndrome
- Boomerang dysplasia
- Bowen-Conradi syndrome
- Brachycephaly deafness cataract mental retardation
- Brachydactyly clinodactyly
- Brachydactyly Smorgasbord type
- Brachydactyly type A3
- Brachydactyly type A5 nail dysplasia
- Brachydactyly type D
- Brachygnathism
- Brachymetatarsia
- Brachyturricephaly
- Branchial arch defects
- Branchial cleft
- Branchial cleft cyst
- Branchial fistula
- Breast aplasia
- Breast hypoplasia
- Brown syndrome
- Brown's
- Brugada syndrome
- Buphthalmos
C
- CAMFAK syndrome
- Camptodactyly
- Camptodactyly joint contractures facial skeletal dysplasia
- Camptodactyly overgrowth unusual facies
- Camptodactyly vertebral fusion
- 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
- CDH
- CDK13-related disorder
- Cebocephaly
- CELSR1
- Central core disease of muscle
- Central nervous system cavernous hemangioma
- Cephalopolysyndactyly
- Cerebral calcification cerebellar hypoplasia
- Cerebral palsy
- Cerebro facio thoracic dysplasia
- Cerebro reno digital syndrome
- Cervical agenesis
- CFC1
- CHAOS
- Char syndrome
- CHARGE association
- Charge syndrome
- CHD
- Chen-Kung Ho–Kaufman–Mcalister syndrome
- Chiari malformation
- Chiari type 1 malformation
- Chitayat–Meunier–Hodgkinson syndrome
- Choanal atresia
- Choledochal cyst
- Choledochal cyst, hand malformation
- Cholestasis pigmentary retinopathy cleft palate
- Chondrodysplasia situs inversus imperforate anus polydactyly
- Christian–Johnson–Angenieta syndrome
- Chromosome 18, trisomy
- Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature
- Circumscribed cutaneous aplasia of the vertex
- Cirsoid aneurysm
- Cleft lip
- Cleft Lip
- Cleft lip and cleft palate
- Cleft lip and palate
- Cleft lip palate abnormal thumbs microcephaly
- Cleft lip palate incisor and finger anomalies
- Cleft lip with or without cleft palate
- Cleft palate
- Cleft Palate
- Cleft palate cardiac defect ectrodactyly
- Cleft palate colobomata radial synostosis deafness
- Cleft palate heart disease polydactyly absent tibia
- Cleft palate incidence by population
- Cleft palate X linked
- Cleft tongue syndrome
- Cleft uvula
- Clefted
- Cloacal septum
- Cloverleaf skull bone dysplasia
