autosomal dominant distal hereditary motor neuronopathy 9

Summary

DOID:0111212 - autosomal dominant distal hereditary motor neuronopathy 9

Disease Ontology 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.

Synonyms: DHMN9, HMN9, distal hereditary motor neuronopathy type 9, distal hereditary motor neuropathy type IX,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: wars1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant distal hereditary motor neuronopathy (is_a)