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Disease Ontology Browser
hereditary spastic paraplegia 52 (DOID:0110804)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 52; CPSQ6; spastic quadriplegic cerebral palsy 6; SPG52
Alt IDs: OMIM:614067, ORDO:280763
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4S1 gene on chromosome 14q12.

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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Send questions and comments to User Support. 		last database update
03/21/2023
MGI 6.22 		The Jackson Laboratory