- OMIM ID
-
609260
- OMIM term:
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2
- Alternative terms:
-
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2
CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A2
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A2
HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA2; HMSN2A2
HMSN IIA2
- (∗) Location:
- 1p36.22
- (†) Associated OMIM genes:
- MFN2
- (‡) Associated MGI genes:
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