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Disease Ontology Browser
hereditary spastic paraplegia 63 (DOID:0110814)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 63; spastic paraplegia 63; SPG63
Alt IDs: OMIM:615686, ICD10CM:G11.4, ORDO:401805
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the AMPD2 gene on chromosome 1p13.


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
02/11/2020
MGI 6.14
The Jackson Laboratory