About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 36 (DOID:0110787)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 36; autosomal dominant spastic paraplegia type 36; SPG36
Alt IDs: OMIM:613096, ICD10CM:G11.4, ORDO:320365
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 12q23-q24.

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, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory