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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: SPG46, autosomal recessive spastic paraplegia 46, autosomal recessive spastic paraplegia type 46,
Xenbase Genes : gba2
MONDO:0013737 - hereditary spastic paraplegia 46 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee