hereditary spastic paraplegia 36

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Echinobase

Summary

Literature (0)

DOID:0110787 - hereditary spastic paraplegia 36

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 12q23-q24.

Synonyms: SPG36, autosomal dominant spastic paraplegia 36, autosomal dominant spastic paraplegia type 36,

Echinobase 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

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)