Human genes for distal hereditary motor neuronopathy type 7
Distal hereditary motor neuronopathy type 7 [DOID:0111199]
An autosomal dominant distal hereditary motor neuronopathy characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis.
Synonyms: distal hereditary motor neuronopathy type 7, distal familial motor neuronopathy type 7, DOID:0111199, dHMN7, DHMNVPy ...