hereditary spastic paraplegia 28 Disease Ontology Browser

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hereditary spastic paraplegia 28 (DOID:0110779)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 28; autosomal recessive spastic paraplegia type 28; SPG28
Alt IDs: OMIM:609340, ICD10CM:G11.4, ORDO:101008
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD1 gene on chromosome 14q22.

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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