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

Xenbase Genes : reep1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012453 - hereditary spastic paraplegia 31

MIM:

MIM:610250 - SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31

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

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