hereditary spastic paraplegia 29 Disease Ontology Browser

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Disease Ontology Browser

hereditary spastic paraplegia 29 (DOID:0110780)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 29; SPG29
Alt IDs: OMIM:609727, ICD10CM:G11.4, ORDO:101009
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1p31.1-p21.1.

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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