About   Help   FAQ
Disease Ontology Browser
hereditary spastic paraplegia 23 (DOID:0110774)
Alliance: disease page
Synonyms: Lison syndrome; Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome; spastic paraplegia 23; spastic paraplegia with pigmentary abnormalities; SPG23
Alt IDs: OMIM:270750, ICD10CM:G11.4, ORDO:101003
Definition: A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32.


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
02/13/2024
MGI 6.23
The Jackson Laboratory