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
02780 CMT2L Charcot-Marie-Tooth disease, type 2L (CMT-2L) 608673 AD 1 1 HSPB8 - -
01447 HMN2A neuropathy, motor, distal, hereditary, type 2A (HMN-2A) 158590 AD - - HSPB8 - -
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