hereditary spastic paraplegia 14 Disease Ontology Browser

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Disease Ontology Browser

hereditary spastic paraplegia 14 (DOID:0110767)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 14; autosomal recessive spastic paraplegia type 14; SPG14
Alt IDs: OMIM:605229, ICD10CM:G11.4, ORDO:100995
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 3q27-q28.

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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