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: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 on chromosome 2q33.

Synonyms: SPG13, autosomal dominant spastic paraplegia 13

In OMIM:
OMIM:605280 - SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT; SPG13

In Mondo Disease Ontology:
MONDO:0011532 - hereditary spastic paraplegia 13

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : hspd1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hereditary spastic paraplegia (is_a)