Summary Literature (0)

DOID:0110797 - hereditary spastic paraplegia 45

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the NT5C2 gene on chromosome 10q24.

Synonyms: SPG45, SPG65, autosomal recessive spastic paraplegia 45, autosomal recessive spastic paraplegia type 45, autosomal recessive spastic paraplegia type 65,

Xenbase Genes : nt5c2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013165 - hereditary spastic paraplegia 45

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee