About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 25 (DOID:0110776)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 25; autosomal recessive spastic paraplegia type 25; SPG25
Alt IDs: OMIM:608220, ICD10CM:G11.4, ORDO:101005
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 6q23-q24.1.

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 6.16
The Jackson Laboratory