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Summary Literature (0)
DOID:13096 - Sneddon syndrome

Disease Ontology 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.

Synonyms: Idiopathic livedo reticularis with systemic involvement, Idiopathic livedo reticularis with systemic involvement (disorder),

Xenbase Genes : ada2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008436 - Sneddon syndrome


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): artery disease (is_a)