- OMIM ID
-
311070
- OMIM term:
- CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5; CMTX5
- Alternative terms:
-
OPTIC ATROPHY, POLYNEUROPATHY, AND DEAFNESS
ROSENBERG-CHUTORIAN SYNDROME
CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED RECESSIVE, 5
- (∗) Location:
- Xq22.3
- (†) Associated OMIM genes:
- PRPS1
- (‡) Associated MGI genes:
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