- OMIM ID
-
607731
- OMIM term:
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H
- Alternative terms:
-
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH PYRAMIDAL FEATURES, AUTOSOMAL RECESSIVE
CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH PYRAMIDAL FEATURES, AUTOSOMAL RECESSIVE
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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