Disease #00770 (AAS;MRX-16 (Aarskog-Scott syndrome (AAS, faciogenital dysplasia, mental retardation, syndromic, X-linked, type 16 (MRX-16)) (AAS)), OMIM:305400)
| Official abbreviation |
AAS;MRX-16 |
| Name |
Aarskog-Scott syndrome (AAS, faciogenital dysplasia, mental retardation, syndromic, X-linked, type 16 (MRX-16)) (AAS) |
| OMIM ID |
305400 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FGD1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
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