hereditary spastic paraplegia 13

Summary

DOID:0110766 - hereditary spastic paraplegia 13

Disease Ontology Definition:A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 gene on chromosome 2q33.

Synonyms: SPG13, autosomal dominant spastic paraplegia 13,

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

: hspd1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011532 - hereditary spastic paraplegia 13

MONDO:0011532 - hereditary spastic paraplegia 13

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)