autosomal dominant distal hereditary motor neuronopathy 3

Summary

DOID:0111207 - autosomal dominant distal hereditary motor neuronopathy 3

Disease Ontology Definition:An autosomal dominant distal hereditary motor neuronopathy that has_material_basis_in heterozygous mutation in the gene encoding heat-shock 27-kD protein-1 (HSPB1) on chromosome 7q11.23.

Synonyms: HMN IIB, HMN2B, distal hereditary motor neuronopathy type 2B, distal hereditary motor neuropathy type IIB,

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

Other Model Organisms: AGR, 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), autosomal dominant distal hereditary motor neuronopathy 2 (is_a)