autosomal dominant distal hereditary motor neuronopathy 6

Summary

DOID:0111210 - autosomal dominant distal hereditary motor neuronopathy 6

Disease Ontology Definition:A distal hereditary motor neuropathy that has_material_basis_in heterozygous mutation in the FBXO38 gene on 5q32.

Synonyms: HMN IID, HMN2D, distal hereditary motor neuronopathy type 2D, distal hereditary motor neuropathy type IID, distal spinal muscular atrophy with calf predominance,

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

: fbxo38

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)