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
02364 CMT2D Charcot-Marie-Tooth disease, type 2D (CMT-2D) 601472 AD 1 1 GARS - -
00195 HMN5A neuropathy, motor, distal, hereditary, type Va (HMN-5A) 600794 AD 23 22 BSCL2, GARS - -
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