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.