All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00014 HMSN Hereditary Sensory and Motor Neuropathy - - 245 - DCAF8, DYNC1H1, EGR2, FGD4, FIG4, GDAP1, GJB1, HSPB2, HSPB8, KIF1B, LITAF, LMNA, MFN2, MPZ, MTMR2, NDRG1, NEFL, PEX7, PHYH, PMP22, 6 more - -
00027 OPA Optic Atrophy 165500 - 296 - AFG3L2, MFN2, OPA1, OPA3, SLC25A46 - -
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