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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

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

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

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