About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 85 (DOID:0112345)
Alliance: disease page
Synonyms: spastic paraplegia 85 autosomal recessive; SPG85
Alt IDs: OMIM:619686
Definition: A hereditary spastic paraplegia characterized by onset of motor symptoms (e.g. spasticity and hyperreflexia of the lower limbs) in the first few years of life that has_material_basis_in homozygous or compound heterozygous mutation in the RNF170 gene on chromosome 8p11.21.


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
02/20/2024
MGI 6.23
The Jackson Laboratory