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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 |