All diseases

OMIM ID
118220
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A; CMT1A
Alternative terms:
HEREDITARY MOTOR AND SENSORY NEUROPATHY IA; HMSN IA
HMSN1A
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1A
CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, WITH FOCALLY FOLDED MYELIN SHEATHS, TYPE 1A
(∗) Location:
17p12  
(†) Associated OMIM genes:
PMP22  
(‡) Associated MGI genes:
Pmp22  

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