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Disease Ontology Browser
hereditary spastic paraplegia 53 (DOID:0110805)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 53; autosomal recessive spastic paraplegia type 53; SPG53
Alt IDs: OMIM:614898, ICD10CM:G11.4, ORDO:319199
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the VPS37A gene on chromosome 8p22.

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
MGI 6.17
The Jackson Laboratory