All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05113 CMT Charcot-Marie-Tooth disease (CMT) - - 957 895 ATP1A1, DHX9, MFN2, MORC2, PLEKHG5, TRIM2, VWA1 - -
03916 CMTRIC Charcot-Marie-Tooth disease, recessive intermediate C (CMTRIC) 615376 AR - - PLEKHG5 - -
03007 DSMA4 atrophy, muscular, spinal, distal, autosomal recessive, type 4 (DSMA-4) 611067 AR - - PLEKHG5 - -
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