All diseases

OMIM ID
607678
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D
Alternative terms:
HEREDITARY MOTOR AND SENSORY NEUROPATHY 1D
HMSN ID
HMSN1D
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1D
(∗) Location:
10q21.3  
(†) Associated OMIM genes:
EGR2  
(‡) Associated MGI genes:

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