hereditary spastic paraplegia 75

Summary

DOID:0110820 - hereditary spastic paraplegia 75

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the MAG gene on chromosome 19q13.

Synonyms: SPG75, autosomal recessive spastic paraplegia 75, autosomal recessive spastic paraplegia type 75,

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

: mag

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014729 - hereditary spastic paraplegia 75

MONDO:0014729 - hereditary spastic paraplegia 75

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)