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
|