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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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory