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Disease Ontology Browser
hereditary spastic paraplegia 42 (DOID:0110794)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 42; autosomal dominant spastic paraplegia type 42; SPG42
Alt IDs: OMIM:612539, ICD10CM:G11.4, ORDO:171863
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the SLC33A1 gene on chromosome 3q25.31.


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
02/18/2020
MGI 6.14
The Jackson Laboratory