Search Ontology:
Human Disease
Sneddon syndrome
- Term ID
- DOID:13096
- Synonyms
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- 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
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- GARD:7664
- MESH:D018860
- MIM:182410
- SNOMEDCT_US_2023_03_01:716745004
- UMLS_CUI:C0282492
- Ontology
- Human Disease ( DOID:13096 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models