Category:Congenital disorders
 | 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.
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Subcategories
This category has the following subcategory, out of 18 total.
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Pages in category "Congenital disorders"
The following 137 pages are in this category, out of approximately 240 total. This list may not reflect recent changes.
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- 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
- Mirror polydactyly-vertebral segmentation-limb defects syndrome
- Monstrous birth
- MORM syndrome
- Muenke syndrome
- Mulibrey nanism
- Multiple abnormalities
- MURCS association
- Muscle–eye–brain disease
- Myelokathexis
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- Palatal obturator
- Papillary fibroelastoma
- Parasitic twin
- Parastremmatic dwarfism
- Patterson syndrome
- Pelvic digit
- Persistent cloaca
- Pfeiffer syndrome
- Phosphate diabetes
- 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
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- 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
- Spondyloperipheral dysplasia
- Status marmoratus
- Strophosomia
- Structural variation
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