All diseases

OMIM ID
601596
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C
Alternative terms:
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE 4C
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4C
(∗) Location:
5q32  
(†) Associated OMIM genes:
SH3TC2  
(‡) Associated MGI genes:
Sh3tc2  

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