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
05113 CMT Charcot-Marie-Tooth disease (CMT) - - 957 895 ATP1A1, DHX9, MFN2, MORC2, PLEKHG5, TRIM2, VWA1 - -
05616 CMT2DD Charcot-Marie-Tooth disease, axonal, type 2DD (CMT-2DD) 618036 AD - - ATP1A1 - autosomal dominant
05617 HOMGSMR2 hypomagnesemia, seizures, and mental retardation type 2 (HOMGSMR-2) 618314 AD - - ATP1A1 - autosomal dominant
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