- OMIM ID
-
601098
- OMIM term:
- CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C
- Alternative terms:
-
CMT, SLOW NERVE CONDUCTION TYPE C
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1C NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE IC
HMSN IC
HMSN1C
- (∗) Location:
- 16p13.13
- (†) Associated OMIM genes:
- LITAF
- (‡) Associated MGI genes:
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