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Disease Ontology Browser
hereditary spastic paraplegia 32 (DOID:0110783)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 32; autosomal recessive spastic paraplegia type 32; SPG32
Alt IDs: OMIM:611252, ICD10CM:G11.4, ORDO:171622
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21.

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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 6.22
The Jackson Laboratory