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Echinobase
Summary Literature (0)
DOID:0110798 - hereditary spastic paraplegia 46

Disease Ontology Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p.

Synonyms: autosomal recessive spastic paraplegia 46, autosomal recessive spastic paraplegia type 46, SPG46

Echinobase Genes : gba2


OMIM:
MIM:614409 - spastic paraplegia 46, autosomal recessive; spg46

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hereditary spastic paraplegia (is_a)