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Disease Ontology Browser
hereditary spastic paraplegia 13 (DOID:0110766)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 13; SPG13
Alt IDs: OMIM:605280, ICD10CM:G11.4, ORDO:100994
Definition: A hereditary spastic paraplegia that is characterized by a pure form of the disease with late onset and has_material_basis_in mutation in the HSPD1 on chromosome 2q33.

Disease References using Mouse Models (1)

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
11/15/2022
MGI 6.22
The Jackson Laboratory