hereditary spastic paraplegia 34 Disease Ontology Browser

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hereditary spastic paraplegia 34 (DOID:0110785)
Alliance: disease page
Synonyms: SPG34; X-linked spastic paraplegia 34; X-linked spastic paraplegia type 34
Alt IDs: OMIM:300750, ICD10CM:G11.4, ORDO:171607
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq24-q25.

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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