About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Copyright, and Privacy Statement
Send questions and comments to User Support.
last database update
01/24/2023
MGI 6.22
The Jackson Laboratory