About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 16 (DOID:0110769)
Alliance: disease page
Synonyms: SPG16; X-linked spastic paraplegia 16; X-linked spastic paraplegia type 16
Alt IDs: OMIM:300266, ICD10CM:G11.4, ORDO:100997
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq11.2.

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 & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.14
The Jackson Laboratory