Version: 8.0.0
Date: Tue Jan 28 2025
Sneddon syndrome
DOID:13096
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

Sneddon syndrome

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
Cross References
Parent Terms
Child Terms
None
Sources of Associations

Associated Genes

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    Associated Alleles

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      Associated Models

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