Search Ontology:
Human Disease

Sneddon syndrome

Term ID
DOID:13096
Synonyms
  • Idiopathic livedo reticularis with systemic involvement
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. https://pubmed.ncbi.nlm.nih.gov/25075847/
References
Ontology
Human Disease   ( DOID:13096 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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