Search Ontology:
Human Disease

autosomal dominant distal hereditary motor neuronopathy

Term ID
DOID:0111198
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 )
Relationships
is a type of
has subtype
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Genes Involved
Zebrafish Models