- OMIM ID
-
600361
- OMIM term:
- HEREDITARY MOTOR AND SENSORY NEUROPATHY V
- Alternative terms:
-
HMSN V
HMSN5
PERONEAL MUSCULAR ATROPHY WITH PYRAMIDAL FEATURES, AUTOSOMAL DOMINANT
CHARCOT-MARIE-TOOTH DISEASE WITH PYRAMIDAL FEATURES, AUTOSOMAL DOMINANT
CHARCOT-MARIE-TOOTH NEUROPATHY WITH PYRAMIDAL FEATURES, AUTOSOMAL DOMINANT
CMT WITH PYRAMIDAL FEATURES
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
Loading mouse genes ...