OBO ID: DOID:0111198
Term Name: autosomal dominant distal hereditary motor neuronopathy Search Ontology:
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. https://www.ncbi.nlm.nih.gov/pubmed/15358725
References:
Ontology: Human Disease   ( DOID:0111198 )
OTHER autosomal dominant distal hereditary motor neuronopathy PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

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