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RUNX1 and myocardial infarction are reported together in 1 article.
Gene
RUNX1
- HGNC
- HGNC:10471
25articles
25mentions
1variants with confirmed gene link
Most co-reported phenotypes (articles)
leukemia 14Down syndrome 2breast cancer 1diabetes mellitus 1hepatocellular carcinoma 1myocardial infarction 1rheumatoid arthritis 1
Reported variants (articles · ClinVar status)
Phenotype
Myocardial infarction
274articles
274mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60Coronary vasospasm in a patient with RUNX1 mutation in eosinophilic leukemia and hypereosinophilic syndrome: A case report.
PMID 41994071 | PMCID PMC13081061 | DOI 10.1016/j.jccase.2026.01.001 · Journal of cardiology cases · 2026 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | RUNX1 | “Coronary vasospasm in a patient with RUNX1 mutation in eosinophilic leukemia and hypereosinophilic syndrome: A case report.” | 0.98 | hgnc_dict_v1 |
| phenotype | myocardial infarction | “RUNX1 also regulates adverse cardiac remodeling after myocardial infarction.” | 0.98 | phenotype_alias_lexicon_v2 |
| phenotype | leukemia | “Coronary vasospasm in a patient with RUNX1 mutation in eosinophilic leukemia and hypereosinophilic syndrome: A case report.” | 0.98 | phenotype_alias_lexicon_v2 |