Category:Congenital disorders
From HandWiki
Here is a list of articles in the category Congenital disorders of the Medicine portal.
 | 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 within Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities 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 3 subcategories, out of 3 total.
C
- Cystic fibrosis (27 P)
T
Pages in category "Congenital disorders"
The following 200 pages are in this category, out of 258 total.
(previous page) (next page)A
- Medicine:Aagenaes syndrome
- Medicine:Aarskog–Scott syndrome
- Medicine:Achondrogenesis
- Medicine:Achondrogenesis type 1B
- Medicine:Achondrogenesis type 2
- Medicine:Achondroplasia
- Medicine:Achondroplasia in children
- Medicine:Acrodysostosis
- Biology:Agenesis
- Medicine:Agenesis
- Medicine:Alcohol and pregnancy
- Biology:Allogeneic processed thymus tissue
- Medicine:Amyoplasia
- Medicine:Anorectal anomalies
- Medicine:Arachnoid cyst
- Medicine:Archibald's sign
- Medicine:Asplenia with cardiovascular anomalies
- Medicine:Atransferrinemia
- Medicine:Autosomal dominant GTP cyclohydrolase I deficiency
- Biology:Autosomal recessive GTP cyclohydrolase I deficiency
- Medicine:Autosomal recessive GTP cyclohydrolase I deficiency
- Medicine:Ayazi syndrome
B
- Medicine:Bangstad syndrome
- Medicine:Barakat syndrome
- Medicine:Bartter syndrome
- Medicine:Benjamin syndrome
- Medicine:Bhaskar–Jagannathan syndrome
- Medicine:Boomerang dysplasia
- Medicine:Bosch-Boonstra-Schaaf optic atrophy syndrome
- Medicine:Bowen–Conradi syndrome
- Medicine:Brugada syndrome
- Medicine:Burnside-Butler syndrome
- Medicine:Burnside–Butler syndrome
C
- Medicine:Arterial calcification due to CD73 deficiency
- Medicine:CAMFAK syndrome
- Medicine:Camptodactyly
- Medicine:CANDLE syndrome
- Medicine:Cat eye syndrome
- Medicine:Caudal duplication
- Medicine:Caudal regression syndrome
- Medicine:Char syndrome
- Medicine:CHERUBS
- Medicine:Animal chimerism
- Medicine:Cleft palate incidence by population
- Biology:Clitoridectomy
- Medicine:Congenital afibrinogenemia
- Biology:Congenital athymia
- Medicine:Congenital athymia
- Medicine:Congenital fiber type disproportion
- Medicine:Congenital hypofibrinogenemia
- Medicine:Congenital iodine deficiency syndrome
- Medicine:Congenital malaria
- Medicine:Congenital nephrotic syndrome
- Medicine:Congenital rubella syndrome
- Medicine:Constriction ring syndrome
- Medicine:Crandall syndrome
- Medicine:Crane-Heise syndrome
- Medicine:Crane–Heise syndrome
- Medicine:Craniofacial team
- Medicine:Craniopagus parasiticus
- Medicine:Crossed beak
- Medicine:Cyclopia
- Medicine:Cystic hygroma
D
E
F
- Medicine:Craniofacial cleft
- Medicine:Facial cleft
- Medicine:Facial femoral syndrome
- Medicine:Faciocardiorenal syndrome
- Medicine:Factor I deficiency
- Medicine:Factor I Deficiency
- Medicine:Familial male-limited precocious puberty
- Medicine:Femur fibula ulna syndrome
- Medicine:Fetal trimethadione syndrome
- Medicine:Fetus in fetu
- Medicine:Fibro-adipose vascular anomaly
- Medicine:Fibrochondrogenesis
- Medicine:Fibrodysplasia ossificans progressiva
- Medicine:Filippi Syndrome
- Medicine:Filippi syndrome
- Medicine:First arch syndrome
- Medicine:Fleischer's syndrome
G
H
- Medicine:Hajdu–Cheney syndrome
- Medicine:Halal syndrome
- Medicine:Halperin-Birk syndrome
- Medicine:Hearing loss with craniofacial syndromes
- Medicine:Hemifacial hypertrophy
- Medicine:Hemifacial microsomia
- Medicine:Heterotopia
- Medicine:Ho–Kaufman–Mcalister syndrome
- Medicine:Holt–Oram syndrome
- Medicine:Hydrolethalus syndrome
- Biology:Hypotransferrinemia
K
L
M
- Medicine:Majewski's polydactyly syndrome
- Biology:Malformative syndrome
- Medicine:Malouf syndrome
- Medicine:Malpuech facial clefting syndrome
- Medicine:Marden–Walker syndrome
- Medicine:Marfanoid
- Medicine:Marinesco–Sjögren syndrome
- Medicine:Mature teratoma
- Medicine:Maturity onset diabetes of the young
- Medicine:Maturity-onset diabetes of the young
- Medicine:McCune–Albright syndrome
- Medicine:MDP syndrome
- Medicine:Meningohydroencephalocoele
- Medicine:Meromelia
- Medicine:Michels syndrome
- Medicine:Miller–Dieker syndrome
- Medicine:Minor physical anomalies
- Medicine:Mirror polydactyly-vertebral segmentation-limb defects syndrome
- Medicine:Monstrous birth
- Medicine:MORM syndrome
- Medicine:Muenke syndrome
- Medicine:Mulibrey nanism
- Medicine:Multiple abnormalities
- Medicine:MURCS association
- Medicine:Muscle–eye–brain disease
- Medicine:Myelokathexis
N
- Medicine:Nager acrofacial dysostosis
- Medicine:Nakajo syndrome
- Medicine:Nasodigitoacoustic syndrome
- Medicine:Neonatal teeth
- Medicine:Neu-Laxova syndrome
- Medicine:Neu–Laxova syndrome
- Biology:Neurocristopathy
- Medicine:Neurocutaneous melanosis
- Medicine:Neuronal ceroid lipofuscinosis
- Medicine:Niemann–Pick disease
- Medicine:Norman–Roberts syndrome
- Medicine:North Carolina macular dystrophy
O
P
- Medicine:Palatal obturator
- Medicine:Papillary fibroelastoma
- Medicine:Parasitic twin
- Medicine:Parastremmatic dwarfism
- Medicine:Patterson syndrome
- Medicine:Pelvic digit
- Medicine:Persistent cloaca
- Medicine:Pfeiffer syndrome
- Medicine:Phosphate diabetes
- Medicine:Pilotto syndrome
- Medicine:Polymelia
- Medicine:Ponseti method
- Medicine:Porencephaly
- Medicine:Potocki–Lupski syndrome
- Medicine:Potocki–Shaffer syndrome
- Medicine:Prader–Willi syndrome
- Medicine:Primary congenital lymphedema
- Medicine:Proboscis (anomaly)
- Medicine:Progressive cardiac conduction defect
- Medicine:Progressive familial intrahepatic cholestasis
- Medicine:Proteus syndrome
- Biology:Pterin-4 alpha-carbinolamine dehydratase deficiency
R
- Medicine:Radioulnar synostosis
- Medicine:Renal dysplasia-limb defects syndrome
- Medicine:Renal hypoplasia
- Medicine:Renal-hepatic-pancreatic dysplasia
- Medicine:Renal–hepatic–pancreatic dysplasia
- Biology:Riboflavin-responsive exercise intolerance
- Medicine:RIDDLE syndrome
- Medicine:Ring chromosome 14 syndrome
- Medicine:Ring chromosome 15
- Medicine:Rosselli–Gulienetti syndrome
- Medicine:Rubinstein–Taybi syndrome
