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Echinobase
Summary Literature (0)
DOID:0110823 - hereditary spastic paraplegia 8

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the KIAA0196 gene on chromosome 8q24.

Synonyms: SPG8, autosomal dominant spastic paraplegia 8, autosomal dominant spastic paraplegia type 8,

Echinobase Genes : washc5


OMIM:
MIM:603563 - spastic paraplegia 8, autosomal dominant; spg8

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)