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
02591 CMT-2F Charcot-Marie-Tooth disease, type 2F (CMT-2F) 606595 - 3 3 HSPB1 - -
02775 HMN-2B neuropathy, motor, distal, hereditary, type 2B (HMN-2B) 608634 - 0 0 HSPB1 - -
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