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Sneddon Syndrome

Disease ID: disease_node_9809

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DbxrefGARD:7664, MESH:D018860, MIM:182410, SNOMEDCT_US_2023_03_01:716745004, UMLS_CUI:C0282492
SubclassofDOID_0050828
Data SourceDOID, MESH
SynonymsIdiopathic livedo reticularis with systemic involvement
Mesh IdD018860
Mesh LabelSneddon Syndrome
Mesh SubclassofD017445, D002561
Doid LabelSneddon syndrome
Doid DescriptionAn 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.
Disease Node Iddisease_node_9809
Doid IdDOID_13096
LabelSneddon Syndrome