Annotation Detail
Information
- Associated Genes
- ADA
- Associated Variants
-
ADA MUTATION
ADA MUTATION - Associated Disease
- Mucocutaneous Lymph Node Syndrome
- Source Database
- DisGeNET
- Description
- These associations include ERAP1, CCR1-CCR3, STAT4, KLRC4, GIMAP4, and TNFAIP3 in Behçet's disease; BLK and CD40 in Kawasaki disease; SERPINA1 and SEMA6A in antineutrophil cytoplasmic antibody associated vasculitides; IL12B and FCGR2A/ FCGR2A in Takayasu arteritis; and CECR1 in a newly defined vascular inflammatory syndrome associated with adenosine deaminase (ADA2) deficiency.
- Pubmed
- 25405820
- Section of the abstract supporting the evidence
- RECENT FINDINGS
- Number of the section of the abstract supporting the evidence
- 2
- Number of the sentence supporting the evidence
- 4
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
Drugs