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Disease Ontology Browser
hereditary spastic paraplegia 30 (DOID:0110781)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 30; autosomal spastic paraplegia type 30; SPG30
Alt IDs: OMIM:610357, ICD10CM:G11.4, ORDO:101010
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF1A gene on chromosome 2q37.

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
MGI 6.19
The Jackson Laboratory