- OMIM ID
-
607706
- OMIM term:
- CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE
- Alternative terms:
-
CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM
CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE
- (∗) Location:
- 8q21.11
- (†) Associated OMIM genes:
- GDAP1
- (‡) Associated MGI genes:
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