FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Sneddon syndrome ID (Ontology) DOID:13096 (Human Disease)
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.
Also Known As "Idiopathic livedo reticularis with systemic involvement"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 Sneddon syndrome       6
 for disease ribbon | Sneddon syndrome       6
 model of | Sneddon syndrome       6
Spanning Tree (Parents/Children)
Only view relationship: 
  vascular disease
   |__artery disease
       |__Sneddon syndrome  6 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a artery disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Idiopathic livedo reticularis with systemic involvement" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:7664
MESH:D018860
MIM:182410
SNOMEDCT_US_2023_03_01:716745004
UMLS_CUI:C0282492