All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02207 MRX99 mental retardation, X-linked, type 99 (MRX99) 300919 XLR 0 0 USP9X - -
06849 MRXS99F Mental retardation, X-linked 99, syndromic, female-restricted 300968 XLD 0 0 USP9X - -
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