hereditary spastic paraplegia 26

Summary

DOID:0110777 - hereditary spastic paraplegia 26

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the B4GALNT1 gene on chromosome 12q13.

Synonyms: GM2 synthase deficiency, SPG26, autosomal recessive spastic paraplegia 26, autosomal recessive spastic paraplegia type 26,

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

: b4galnt1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012213 - hereditary spastic paraplegia 26

MONDO:0012213 - hereditary spastic paraplegia 26

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

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

Parent(s): autosomal recessive disease (is_a), hereditary spastic paraplegia (is_a)