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
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 - -
00034 SMA Spinal Muscular Atrophy 253300 - 90 - HEXA, IGHMBP2, LMNA, SMN1, VAPB - -
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