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hereditary spastic paraplegia 51 (DOID:0110803)
Alliance: disease page
Synonyms: autosomal dominant spastic paraplegia 51; CPSQ4; spastic quadriplegic cerebral palsy 4; SPG51
Alt IDs: OMIM:613744, ORDO:280763
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4E1 gene on chromosome 15q21.


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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last database update
01/17/2023
MGI 6.22
The Jackson Laboratory