Term Name: autosomal dominant distal hereditary motor neuronopathy
Synonyms: autosomal dominant dHMN, autosomal dominant distal hereditary motor neuropathy, autosomal dominant distal spinal muscular atrophy
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.
Ontology: Human Disease [DOID:0111198]   ( DOID:0111198 )

Relationships
is a type of: autosomal dominant disease spinal muscular atrophy
has subtype: autosomal dominant distal hereditary motor neuronopathy 1 autosomal dominant distal hereditary motor neuronopathy 2 autosomal dominant distal hereditary motor neuronopathy 3 autosomal dominant distal hereditary motor neuronopathy 4 autosomal dominant distal hereditary motor neuronopathy 5 autosomal dominant distal hereditary motor neuronopathy 6 autosomal dominant distal hereditary motor neuronopathy 7 autosomal dominant distal hereditary motor neuronopathy 8 autosomal dominant distal hereditary motor neuronopathy 9 autosomal dominant distal hereditary motor neuronopathy 10 autosomal dominant distal hereditary motor neuronopathy 11 autosomal dominant distal hereditary motor neuronopathy 12 autosomal dominant distal hereditary motor neuronopathy 13 autosomal dominant distal hereditary motor neuronopathy 14