All diseases

OMIM ID
118210
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1
Alternative terms:
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1
CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1
HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1
HMSN IIA1
HMSN2A1
(∗) Location:
1p36.22  
(†) Associated OMIM genes:
KIF1B  
(‡) Associated MGI genes:
Kif1b  

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