hereditary spastic paraplegia 16 Disease Ontology Browser

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Disease Ontology Browser

hereditary spastic paraplegia 16 (DOID:0110769)
Alliance: disease page
Synonyms: SPG16; X-linked spastic paraplegia 16; X-linked spastic paraplegia type 16
Alt IDs: OMIM:300266, ICD10CM:G11.4, ORDO:100997
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq11.2.

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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