About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 7 (DOID:0110816)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 7; spastic paraplegia type 7; SPG7
Alt IDs: OMIM:607259, ICD10CM:G11.4, ORDO:99013
Definition: A hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-60 years of age, and generally more severe spasticity and has_material_basis_in mutation in the SPG7 gene on chromosome 16q24.

Disease References using Mouse Models (2)

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
03/12/2024
MGI 6.23
The Jackson Laboratory