Summary Literature (0)

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

Xenbase Genes : kif5a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011408 - hereditary spastic paraplegia 10

MIM:

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