About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 30 (DOID:0110781)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 30; autosomal recessive spastic paraplegia 30; autosomal spastic paraplegia type 30; SPG30
Alt IDs: OMIM:610357, ICD10CM:G11.4, ORDO:101010
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF1A gene on chromosome 2q37.

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, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory