autosomal dominant distal hereditary motor neuronopathy 2

Summary

DOID:0111206 - autosomal dominant distal hereditary motor neuronopathy 2

Disease Ontology 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.

Synonyms: HMN II, HMN IIA, HMN2, HMN2A, autosomal dominant adult spinal muscular atrophy IIA, distal hereditary motor neuronopathy type 2, distal hereditary motor neuronopathy type 2A, distal hereditary motor neuropathy type II, distal hereditary motor neuropathy type IIA, spinal Charcot-Marie-Tooth disease IIA,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: hspb1, hspb8

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant distal hereditary motor neuronopathy (is_a)