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:0110793 - hereditary spastic paraplegia 41

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2.

Synonyms: SPG41, autosomal dominant spastic paraplegia 41, autosomal dominant spastic paraplegia type 41,

Echinobase Genes :



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)