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Disease Ontology Browser
hereditary spastic paraplegia 51 (DOID:0110803)
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/15/2017
MGI 6.10
The Jackson Laboratory