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Disease Ontology Browser
hereditary spastic paraplegia 48 (DOID:0110800)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 48; autosomal recessive spastic paraplegia type 48; SPG48
Alt IDs: OMIM:613647, ICD10CM:G11.4, ORDO:306511
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the AP5Z1 gene on chromosome 7p22.1.

Disease References using Mouse Models (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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11/12/2024
MGI 6.24 		The Jackson Laboratory