Sneddon Syndrome
Disease ID: disease_node_9809
Connections displayed (default: 10).
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| Dbxref | GARD:7664, MESH:D018860, MIM:182410, SNOMEDCT_US_2023_03_01:716745004, UMLS_CUI:C0282492 |
|---|---|
| Subclassof | DOID_0050828 |
| Data Source | DOID, MESH |
| Synonyms | Idiopathic livedo reticularis with systemic involvement |
| Mesh Id | D018860 |
| Mesh Label | Sneddon Syndrome |
| Mesh Subclassof | D017445, D002561 |
| Doid Label | Sneddon syndrome |
| Doid Description | 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. |
| Disease Node Id | disease_node_9809 |
| Doid Id | DOID_13096 |
| Label | Sneddon Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Artery Disease(ID:disease_node_13138) (Disease)