About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 48 (DOID:0110800)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 48; autosomal recessive spastic paraplegia type 48; SPG48
Alt IDs: OMIM:613647, ICD10CM:G11.4, ORDO:306511
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the AP5Z1 gene on chromosome 7p22.1.

Disease References using Mouse Models (1)

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
MGI 6.20
The Jackson Laboratory