All diseases

4 entries on 1 page. Showing entries 1 - 4.
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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 - -
00199 CMT2 Charcot-Marie-Tooth disease, type 2 (CMT-2) - - 239 158 MORC2 - -
05791 CMT2Z Charcot-Marie-Tooth disease, type 2Z (CMT2Z) 616688 AD 2 1 MORC2 - -
07047 DIGFAN developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy 619090 AD - - MORC2 - -
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