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Disease Ontology Browser
hereditary spastic paraplegia 31 (DOID:0110782)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 31; autosomal dominant spastic paraplegia type 31; SPG31
Alt IDs: OMIM:610250, ICD10CM:G11.4, ORDO:101011
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP1 gene on chromosome 2p11.

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 6.22
The Jackson Laboratory