- OMIM ID
-
182960
- OMIM term:
- NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I; HMN1
- Alternative terms:
-
HMN I
NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE I
DHMN1
SPINAL MUSCULAR ATROPHY, DISTAL, JUVENILE, AUTOSOMAL DOMINANT, I
CHARCOT-MARIE-TOOTH DISEASE, SPINAL, I
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
Loading mouse genes ...