Term Name:	autosomal dominant distal hereditary motor neuronopathy 5
Synonyms:	DHMN5, distal hereditary motor neuronopathy type 5, distal hereditary motor neuronopathy type 5A, distal hereditary motor neuropathy type V, distal HMN V, distal spinal muscular atrophy type V, distal spinal muscular atrophy with upper limb predominance, DSMAV, HMN5
Definition:	An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of distal muscle weakness and atrophy predominantly affecting the upper limbs in the first few decades of life and that has_material_basis_in heterozygous mutation in the GARS gene on chromosome 7p14.
Ontology:	Human Disease [DOID:0111203]   ( DOID:0111203 )