hereditary spastic paraplegia 10

Summary

DOID:0110763 - hereditary spastic paraplegia 10

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF5A gene on chromosome 12q13.

Synonyms: autosomal dominant spastic paraplegia 10, autosomal dominant spastic paraplegia type 10, SPG10

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

: kif5a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011408 - hereditary spastic paraplegia 10

MONDO:0011408 - hereditary spastic paraplegia 10

MIM:

MIM:604187 - SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10

MIM:604187 - SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10

Other Model Organisms: Alliance, 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)