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Disease Ontology Browser
hereditary spastic paraplegia 8 (DOID:0110823)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 8; autosomal dominant spastic paraplegia type 8; SPG8
Alt IDs: OMIM:603563, ICD10CM:G11.4, ORDO:100989
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the KIAA0196 gene on chromosome 8q24.

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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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory