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, and Privacy Statement
Send questions and comments to User Support.
last database update
01/24/2023
MGI 6.22
The Jackson Laboratory