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Disease Ontology Browser
hereditary spastic paraplegia 46 (DOID:0110798)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 46; autosomal recessive spastic paraplegia type 46; SPG46
Alt IDs: OMIM:614409, ICD10CM:G11.4, ORDO:320391
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the GBA2 gene on chromosome 9p.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
02/11/2020
MGI 6.14
The Jackson Laboratory