- OMIM ID
-
607831
- OMIM term:
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K
- Alternative terms:
-
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2K
CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, TYPE 2K CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, TYPE 2K, INCLUDED
- (∗) Location:
- 8q21.11
- (†) Associated OMIM genes:
- GDAP1
- (‡) Associated MGI genes:
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