- OMIM ID
-
609311
- OMIM term:
- CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H
- Alternative terms:
-
CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL RECESSIVE, TYPE 4H
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE 4H
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4H
- (∗) Location:
- 12p11.21
- (†) Associated OMIM genes:
- FGD4
- (‡) Associated MGI genes:
Loading mouse genes ...