All diseases

OMIM ID
302800
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1
Alternative terms:
CMTX
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED
HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED
HMSN, X-LINKED
CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1
CMT2, FORMERLY
(∗) Location:
Xq13.1  
(†) Associated OMIM genes:
GJB1  
(‡) Associated MGI genes:
Gjb1  

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