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
05113 CMT Charcot-Marie-Tooth disease (CMT) - - 1095 1033 ATP1A1, DHX9, MFN2, MORC2, PLEKHG5, TRIM2, VWA1 - -
07240 HMNR7 neuronopathy, distal hereditary motor, autosomal recessive, type 7 611901 AR - - VWA1 - -
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