- OMIM ID
-
214370
- OMIM term:
- NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, MENTAL RETARDATION, AND ABSENT SENSORY LARGE MYELINATED FIBERS
- Alternative terms:
-
CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS
DEAFNESS WITH CHARCOT-MARIE-TOOTH DISEASE
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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