Term Name:	autosomal dominant distal hereditary motor neuronopathy 2
Synonyms:	distal hereditary motor neuronopathy type 2, distal hereditary motor neuronopathy type 2A, distal hereditary motor neuropathy type II, HMN II, HMN2
Definition:	An autosomal dominant distal hereditary motor neuronopathy that is characterized by onset of slowly progressive distal limb weakness and atrophy between the second and fifth decades of life.
Ontology:	Human Disease [DOID:0111206]   ( DOID:0111206 )