Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110782 - hereditary spastic paraplegia 31

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11.

Synonyms: SPG31, autosomal dominant spastic paraplegia 31, autosomal dominant spastic paraplegia type 31,

Xenbase Genes : reep1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012453 - hereditary spastic paraplegia 31

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), hereditary spastic paraplegia (is_a)