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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)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory