- OMIM ID
-
158590
- OMIM term:
- NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA; HMN2A
- Alternative terms:
-
HMN IIA
NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA
DHMN2A
SPINAL MUSCULAR ATROPHY, DISTAL, ADULT, AUTOSOMAL DOMINANT, IIA
CHARCOT-MARIE-TOOTH DISEASE, SPINAL, IIA
- (∗) Location:
- 12q24.23
- (†) Associated OMIM genes:
- HSPB8
- (‡) Associated MGI genes:
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