hereditary spastic paraplegia 31

Summary

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 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

: reep1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012453 - hereditary spastic paraplegia 31

MONDO:0012453 - hereditary spastic paraplegia 31

Other Model Organisms: AGR, 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)