autosomal dominant distal hereditary motor neuronopathy (DOID:0111198)
Alliance: disease page
Synonyms: autosomal dominant dHMN; autosomal dominant distal hereditary motor neuropathy; autosomal dominant distal spinal muscular atrophy
Alt IDs: OMIM:PS182960, ORDO:140465
Definition: A spinal muscular atrophy that is characterized by progressive distal motor weakness and muscular atrophy of the peripheral nervous system without sensory impairment, that is caused by anterior horn cell degeneration, and that has_material_basis_in autosomal dominant inheritance.