About   Help   FAQ
Disease Ontology Browser
Sneddon syndrome (DOID:13096)
Alliance: disease page
Synonyms: Idiopathic livedo reticularis with systemic involvement
Alt IDs: OMIM:182410, MESH:D018860, UMLS_CUI:C0282492
Definition: An artery disease that is characterized by onset of livedo reticularis in the second decade and onset of cerebrovascular disease in early adulthood and that has_material_basis_in compound heterozygous mutation in the CECR1 gene (ADA2) on chromosome 22q11.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory