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 (22 P)
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Pages in category "Congenital disorders"
The following 133 pages are in this category, out of 133 total.
A
B
C
D
F
H
M
- Biology:Malformative syndrome
- Medicine:Malpuech facial clefting syndrome
- Medicine:Marden–Walker syndrome
- Medicine:Marinesco–Sjögren syndrome
- Medicine:Mature teratoma
- Medicine:Maturity-onset diabetes of the young
- Medicine:McCune–Albright syndrome
- Medicine:MDP syndrome
- Medicine:Michels syndrome
- Medicine:Miller–Dieker syndrome
- Medicine:Mirror polydactyly-vertebral segmentation-limb defects syndrome
- Medicine:MORM syndrome
- Medicine:Muenke syndrome
- Medicine:Mulibrey nanism
- Medicine:MURCS association
- Medicine:Myelokathexis
N
O
P
- Medicine:Palatal obturator
- Medicine:Papillary fibroelastoma
- Medicine:Parasitic twin
- Medicine:Parastremmatic dwarfism
- Medicine:Patterson syndrome
- Medicine:Pfeiffer syndrome
- Medicine:Pilotto syndrome
- Medicine:Polymelia
- Medicine:Ponseti method
- Medicine:Potocki–Shaffer syndrome
- Medicine:Progressive cardiac conduction defect
- Medicine:Progressive familial intrahepatic cholestasis
- Medicine:Proteus syndrome
R
S
- Medicine:Sacrococcygeal teratoma
- Medicine:Saethre–Chotzen syndrome
- Medicine:Senior–Løken syndrome
- Medicine:Sepiapterin reductase deficiency
- Medicine:Simpson–Golabi–Behmel syndrome
- Medicine:Sirenomelia
- Medicine:Situs inversus
- Medicine:Smith–Fineman–Myers syndrome
- Medicine:Spondyloepimetaphyseal dysplasia, Strudwick type
- Biology:Structural variation
