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
02587 CMTDIB;CMT2M Charcot-Marie-Tooth disease, dominant intermediate, type B (CMTDIB, axonal, type 2M (CMT-2M)) 606482 AD 1 1 DNM2 - -
01454 CNM1 myopathy, centronuclear, type 1 (CNM1) 160150 AD 44 44 DNM2, MTMR14 - -
03911 LCCS5 contracture syndrome, lethal, congenital, type 5 (LCCS-5) 615368 AR 0 0 DNM2 - -
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