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DO Term : autosomal dominant distal hereditary motor neuronopathy 9 [DOID:0111212] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • HMN9,
  • 617721,
  • distal hereditary motor neuropathy type IX,
  • DHMN9,
  • distal hereditary motor neuronopathy type 9,
  • OMIM:617721
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents