- OMIM ID
-
310490
- OMIM term:
- COWCHOCK SYNDROME
- Alternative terms:
-
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 4; CMTX4
CHARCOT-MARIE-TOOTH DISEASE WITH DEAFNESS AND MENTAL RETARDATION
NEUROPATHY, AXONAL MOTOR-SENSORY, WITH DEAFNESS AND MENTAL RETARDATION; NAMSD
NADMR
- (∗) Location:
- Xq24-q26.1
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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