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Disease Ontology Browser
hereditary spastic paraplegia 72 (DOID:0110817)
Alliance: disease page
Synonyms: autosomal spastic paraplegia type 72; SPG72
Alt IDs: OMIM:615625, ICD10CM:G11.4, ORDO:401849
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the REEP2 gene on chromosome 5q31.


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
02/04/2020
MGI 6.14
The Jackson Laboratory