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Disease Ontology Browser
hereditary spastic paraplegia 12 (DOID:0110765)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 12; autosomal dominant spastic paraplegia type 12; SPG12
Alt IDs: OMIM:604805, ICD10CM:G11.4, ORDO:100993
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the RTN2 gene on chromosome 19q13.

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 6.14
The Jackson Laboratory