All diseases

OMIM ID
601382
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1
Alternative terms:
CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL RECESSIVE, WITH FOCALLY FOLDED MYELIN SHEATHS, AUTOSOMAL RECESSIVE, TYPE 4B1
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4B1
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B; CMT4B
(∗) Location:
11q21  
(†) Associated OMIM genes:
MTMR2  
(‡) Associated MGI genes:
Mtmr2  

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