All diseases

OMIM ID
605588
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1
Alternative terms:
CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2B1
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, B1
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2B1
(∗) Location:
1q22  
(†) Associated OMIM genes:
LMNA  
(‡) Associated MGI genes:
Lmna  

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