- OMIM ID
-
606071
- OMIM term:
- HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C
- Alternative terms:
-
HMSN IIC
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2C; CMT2C
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2C
- (∗) Location:
- 12q24.11
- (†) Associated OMIM genes:
- TRPV4
- (‡) Associated MGI genes:
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