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
05528 MRD41 mental retardation, autosomal dominant, type 41 (MRD-41) 616944 AD - - TBL1XR1 - autosomal dominant
05529 PRPTS Pierpont syndrome (PRPTS) 602342 AD - - TBL1XR1 - autosomal dominant
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