All diseases associated with gene FGD1

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

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 - - - - -
00139 ID intellectual disability (ID) - - - - - -
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