About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/18/2020
MGI 6.14
The Jackson Laboratory