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
04514 CMT2S Charcot-Marie-Tooth disease, axonal, type 2S (CMT-2S) 616155 AR 1 1 IGHMBP2 - -
02496 DSMA1 atrophy, muscular, spinal, distal, type 1 (DSMA-1, alias SMARD-1) 604320 AR 68 69 IGHMBP2 - -
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