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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 18/11/2005 |
Symbol | CDAGS |
Location | 22q12-q13 |
Name | CDAGS syndrome |
Other name(s) |
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Main clinical features |
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Genetic determination | autosomal recessive |
Function/system disorder | osteo-articular |
sex-genitalia | |
dermatology | |
digestive tract/liver and annex | |
Type | malformation |