autosomal dominant distal hereditary motor neuronopathy 9 (DOID:0111212)
Alliance: disease page
Synonyms: DHMN9; distal hereditary motor neuronopathy type 9; distal hereditary motor neuropathy type IX; HMN9
Alt IDs: OMIM:617721
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.