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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)
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last database update
MGI 6.23
The Jackson Laboratory