All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00770 AAS;MRX-16 Aarskog-Scott syndrome (AAS, faciogenital dysplasia, mental retardation, syndromic, X-linked, type 16 (MRX-16)) (AAS) 305400 37 37 FGD1 - -