Disease #00014 (HMSN (Hereditary Sensory and Motor Neuropathy))
Official abbreviation |
HMSN |
Name |
Hereditary Sensory and Motor Neuropathy |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
245 |
Phenotype entries for this disease |
- |
Associated with 26 genes |
DCAF8, DYNC1H1, EGR2, FGD4, FIG4, GDAP1, GJB1, HSPB2, HSPB8, KIF1B, LITAF, LMNA, MFN2, MPZ, MTMR2, NDRG1, NEFL, PEX7, PHYH, PMP22, 6 more...DCAF8, DYNC1H1, EGR2, FGD4, FIG4, GDAP1, GJB1, HSPB2, HSPB8, KIF1B, LITAF, LMNA, MFN2, MPZ, MTMR2, NDRG1, NEFL, PEX7, PHYH, PMP22, PRX, RAB7A, SBF2, SH3TC2, SLC12A6, TFG |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
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