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Disease Ontology Browser
hereditary spastic paraplegia 84 (DOID:0112347)
Alliance: disease page
Synonyms: spastic paraplegia 84 autosomal recessive; SPG84
Alt IDs: OMIM:619621
Definition: A hereditary spastic paraplegia characterized by onset in the first 2 decades of life of slowly progressive walking difficulties due to lower limb weakness, stiffness, and spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the PI4KA gene on chromosome 22q11.21.

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