Search Ontology:
Human Disease

autosomal dominant distal hereditary motor neuronopathy 9

Term ID
DOID:0111212
Synonyms
  • DHMN9
  • distal hereditary motor neuronopathy type 9
  • distal hereditary motor neuropathy type IX
  • HMN9
Definition
An autosomal domiant distal hereditary motor neuronopathy that is characterized by juvenile onset of slowly progressive distal muscle weakness and atrophy affecting both the lower and upper limbs that has_material_basis_in heterozygous mutation in the WARS gene on 14q32.2. https://www.ncbi.nlm.nih.gov/pubmed/28369220
References
Ontology
Human Disease   ( DOID:0111212 )
Relationships
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Genes Involved
Zebrafish Models