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
04445 CMT2T Charcot-Marie-Tooth disease,? axonal, type 2T (CMT-2T) 616233 - 1 1 DNAJB2 - -
03773 DSMA5 atrophy, muscular, spinal, distal, autosomal recessive, type 5 (DSMA-5) 614881 AR - - DNAJB2 - -
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