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 (25 P)
T
Pages in category "Congenital disorders"
The following 163 pages are in this category, out of 163 total.
A
- Medicine:Aagenaes syndrome
- Medicine:Achondrogenesis type 1B
- Medicine:Achondrogenesis type 2
- Medicine:Achondroplasia
- Medicine:Acrodysostosis
- Biology:Agenesis
- Medicine:Alcohol and pregnancy
- Medicine:Ampola syndrome
- Medicine:Arachnoid cyst
- Medicine:Asplenia with cardiovascular anomalies
- Medicine:Atransferrinemia
- Medicine:Autosomal dominant GTP cyclohydrolase I deficiency
B
C
- Medicine:Arterial calcification due to CD73 deficiency
- Medicine:CAMFAK syndrome
- Medicine:CANDLE syndrome
- Medicine:Caudal regression syndrome
- Biology:Chromosome No. 1 syndrome
- Biology:Clitoridectomy
- Medicine:Complex vertebral malformation
- Medicine:Congenital hypofibrinogenemia
- Medicine:Congenital rubella syndrome
- Medicine:Craniopagus parasiticus
D
E
F
- Medicine:Craniofacial cleft
- Medicine:Facial cleft
- Medicine:Factor I deficiency
- Medicine:Familial male-limited precocious puberty
- Medicine:Fetal alcohol spectrum disorder
- Medicine:Fetal trimethadione syndrome
- Medicine:Fetus in fetu
- Medicine:Fibrinogen deficiency
- Medicine:Fibrochondrogenesis
- Medicine:Fibrodysplasia ossificans progressiva
- Medicine:Filippi Syndrome
- Medicine:Filippi syndrome
G
H
M
- Biology:Malformative syndrome
- Medicine:Malouf 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:Mosaic variegated aneuploidy syndrome
- Medicine:Muenke syndrome
- Medicine:Mulibrey nanism
- Medicine:Multiple abnormalities
- 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–Lupski syndrome
- Medicine:Potocki–Shaffer syndrome
- Medicine:Progressive cardiac conduction defect
- Medicine:Progressive familial intrahepatic cholestasis
- Medicine:Proteus syndrome
R
- 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:Ring chromosome 14 syndrome
- Medicine:Ring chromosome 15
- Medicine:Rosselli–Gulienetti syndrome
- Medicine:Rudiger syndrome
S
- Medicine:Sacral dimple
- Medicine:Sacrococcygeal teratoma
- Medicine:Saethre–Chotzen syndrome
- Medicine:Seckel syndrome
- Medicine:Senior–Løken syndrome
- Medicine:Sepiapterin reductase deficiency
- Medicine:SHORT syndrome
- Medicine:Simpson–Golabi–Behmel syndrome
- Medicine:Sirenomelia
- Medicine:Situs inversus
- Medicine:Smith–Fineman–Myers syndrome
- Medicine:Spondyloepimetaphyseal dysplasia, Strudwick type
- Biology:Structural variation
T
- Medicine:Tay–Sachs disease
- Medicine:Teratoma
- Medicine:Tetra-amelia syndrome
- Medicine:Thumb hypoplasia
- Medicine:TORCH syndrome
- Biology:Toxocara malayasiensis
- Medicine:Trichothiodystrophy
- Medicine:Triphalangeal thumb
- Medicine:Triple-A syndrome
- Medicine:Triploid syndrome
- Biology:Tyrosine hydroxylase deficiency
