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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:0008436 - Sneddon syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
artery disease (is_a)