All diseases

5 entries on 1 page. Showing entries 1 - 5.
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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 - -
05176 CMT2A2A Charcot-Marie-Tooth disease, type 2A2A (CMT2A2A) 609260 AD 59 2 MFN2 - -
05889 CMT2A2B Charcot-Marie-Tooth disease, type 2A2B (CMT2A2B) 617087 AR - - MFN2 - -
02342 HMSN6A neuropathyneuropathy, motor and sensory, hereditary, with optic atrophy, type6A (HMSN6A) 601152 AD - - MFN2 - -
05684 neuropathy, optic neuropathy, optic - - 314 298 ACO2, DNM1L, MFN2, NR2F1, OPA1, RTN4IP1, SPG7, SSBP1 - -
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