Category:Congenital disorders
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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.
Wikimedia Commons has media related to Congenital disorders.
Subcategories
This category has the following 19 subcategories, out of 19 total.
A
- Albinism (5 C, 12 P)
C
- Congenital disorders of circulatory system (2 C, 3 P)
- Congenital disorders of digestive system (1 C, 34 P)
- Congenital disorders of eye, ear, face and neck (2 C, 18 P)
- Congenital disorders of genital organs (3 C, 10 P)
- Congenital disorders of musculoskeletal system (4 C, 143 P)
- Congenital disorders of nervous system (6 C, 59 P)
- Cutaneous congenital anomalies (1 C, 104 P)
- Cystic fibrosis (3 C, 28 P)
E
- Ehlers–Danlos syndrome (1 C, 5 P)
I
- Inborn errors of metabolism (17 C, 27 P)
T
- Teratogens (12 C, 47 P)
Pages in category "Congenital disorders"
The following 200 pages are in this category, out of approximately 237 total. This list may not reflect recent changes.
(previous page) (next page)A
- Aagenaes syndrome
- Aarskog–Scott syndrome
- Achondrogenesis
- Achondrogenesis type 1B
- Achondrogenesis type 2
- Achondroplasia
- Achondroplasia in children
- Acrodysostosis
- Agenesis
- Alcohol and pregnancy
- Allogeneic processed thymus tissue
- Amyoplasia
- Anorectal anomalies
- Arachnoid cyst
- Archibald's sign
- Asplenia with cardiovascular anomalies
- Atransferrinemia
- Autosomal dominant GTP cyclohydrolase I deficiency
- Autosomal recessive GTP cyclohydrolase I deficiency
- Ayazi syndrome
B
C
- Arterial calcification due to CD73 deficiency
- CAMFAK syndrome
- Camptodactyly
- CANDLE syndrome
- Cat eye syndrome
- Caudal duplication
- Caudal regression syndrome
- Char syndrome
- Animal chimerism
- Cleft palate incidence by population
- Clitoridectomy
- Congenital afibrinogenemia
- Congenital athymia
- Congenital fiber type disproportion
- Congenital hypofibrinogenemia
- Congenital iodine deficiency syndrome
- Congenital malaria
- Congenital nephrotic syndrome
- Congenital rubella syndrome
- Constriction ring syndrome
- Crandall syndrome
- Crane-Heise syndrome
- Craniopagus parasiticus
- Cyclopia
- Cystic hygroma
D
E
F
- Craniofacial cleft
- Facial femoral syndrome
- Faciocardiorenal syndrome
- Factor I deficiency
- Familial male-limited precocious puberty
- Femur fibula ulna syndrome
- Fetal trimethadione syndrome
- Fetus in fetu
- Fibro-adipose vascular anomaly
- Fibrochondrogenesis
- Fibrodysplasia ossificans progressiva
- Filippi syndrome
- First arch syndrome
- Fleischer's syndrome
G
H
M
- Majewski's polydactyly syndrome
- Malformative syndrome
- Malouf syndrome
- Malpuech facial clefting syndrome
- Marden–Walker syndrome
- Marfanoid
- Marinesco–Sjögren syndrome
- Maturity-onset diabetes of the young
- McCune–Albright syndrome
- MDP syndrome
- Meningohydroencephalocoele
- Meromelia
- Michels syndrome
- Miller–Dieker syndrome
- Minor physical anomalies
- Monstrous birth
- MORM syndrome
- Muenke syndrome
- Mulibrey nanism
- Multiple abnormalities
- MURCS association
- Muscle–eye–brain disease
- Myelokathexis
N
O
P
- Palatal obturator
- Papillary fibroelastoma
- Parasitic twin
- Parastremmatic dwarfism
- Patterson syndrome
- Pelvic digit
- Persistent cloaca
- Pfeiffer syndrome
- Pilotto syndrome
- Polymelia
- Ponseti method
- Porencephaly
- Potocki–Lupski syndrome
- Potocki–Shaffer syndrome
- Prader–Willi syndrome
- Primary congenital lymphedema
- Proboscis (anomaly)
- Progressive cardiac conduction defect
- Progressive familial intrahepatic cholestasis
- Proteus syndrome
- Pterin-4 alpha-carbinolamine dehydratase deficiency
R
S
- Sacral agenesis
- Sacral dimple
- Sacrococcygeal teratoma
- Saethre–Chotzen syndrome
- Seckel syndrome
- Senior–Løken syndrome
- Sepiapterin reductase deficiency
- Sequence (medicine)
- SHORT syndrome
- Shprintzen–Goldberg syndrome
- Simpson–Golabi–Behmel syndrome
- Sirenomelia
- Situs ambiguus
- Situs inversus
- Smith–Fineman–Myers syndrome
- Snyder–Robinson syndrome
- Spondyloepimetaphyseal dysplasia
- Spondyloepimetaphyseal dysplasia, Strudwick type