Term Name:	autosomal dominant distal hereditary motor neuronopathy 14
Synonyms:	DHMN7B, distal hereditary motor neuronopathy type 7B, distal hereditary motor neuropathy type VIIB, distal spinal muscular atrophy with vocal cord paralysis type 7B, Harper-Young myopathy, HMN VIIB, HMN7B
Definition:	An autosomal dominant distal hereditary motor neuronopathy that has_material_basis_in heterozygous mutation in the DCTN1 gene on 2p13.1.
Ontology:	Human Disease [DOID:0111202]   ( DOID:0111202 )