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
06483 CMT2EE Charcot-Marie-Tooth disease, axonal, type 2EE 618400 AR - - MPV17 - -
00320 MTDPS6 mitochondrial DNA depletion syndrome (hepatocerebral), type 6 (MTDPS-6) 256810 AR 10 10 MPV17 - -
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