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Disease Ontology Browser
hereditary spastic paraplegia 52 (DOID:0110804)
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory