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Metadata
ID DOID:0111199
Name distal hereditary motor neuronopathy type 7
Definition 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.
https://www.ncbi.nlm.nih.gov/pubmed/7420092
Xrefs

ORDO:139589

Synonyms

dHMN7 [EXACT]

DHMNVPy [EXACT]

distal spinal muscular atrophy with vocal cord paralysis [EXACT]

Parent Relationships

is_a autosomal dominant distal hereditary motor neuronopathy

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