hereditary spastic paraplegia 15

Summary

DOID:0110768 - hereditary spastic paraplegia 15

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1.

Synonyms: Kjellin syndrome, SPG15, autosomal recessive spastic paraplegia 15, autosomal recessive spastic paraplegia type 15, hereditary spastic paraparesis type 15, spastic paraplegia and retinal degeneration, spastic paraplegia-retinal degeneration syndrome,

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

: zfyve26

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010044 - hereditary spastic paraplegia 15

MONDO:0010044 - hereditary spastic paraplegia 15

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

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

Parent(s): autosomal recessive disease (is_a), hereditary spastic paraplegia (is_a)