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Disease Ontology Browser
hereditary spastic paraplegia 2 (DOID:0110773)
Alliance: disease page
Synonyms: spastic paraplegia type 2; SPG2; X-linked spastic paraplegia 2
Alt IDs: OMIM:312920, ICD10CM:G11.4, ORDO:99015
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.

Disease References using Mouse Models (2)

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
10/08/2019
MGI 6.14
The Jackson Laboratory