About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 72A (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 a heterozygous mutation in the REEP2 gene on chromosome 5q31.2.

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, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory