Term Name:	autosomal dominant distal hereditary motor neuronopathy 9
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.
Ontology:	Human Disease [DOID:0111212]   ( DOID:0111212 )