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
05756 CNM6 myopathy, centronuclear, type 6, with fiber-type disproportion (CNM6) 617760 AR - - MAP3K20 - -
05757 SFMMP split-foot malformation with mesoaxial polydactyly (SFMMP) 616890 AR - - MAP3K20 - -
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