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
00765 CLS syndrome, Coffin-Lowry (CLS) 303600 - 0 0 RPS6KA3 - X-linked dominant
00766 MRX-19 mental retardation, X-linked, type 19 (MRX-19) 300844 - 0 0 RPS6KA3 - -
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