- OMIM ID
-
600882
- OMIM term:
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B
- Alternative terms:
-
CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, TYPE 2B
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2B
HEREDITARY MOTOR AND SENSORY NEUROPATHY IIB; HMSN IIB
HMSN2B
- (∗) Location:
- 3q21.3
- (†) Associated OMIM genes:
- RAB7
- (‡) Associated MGI genes:
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