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Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.
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Phenotype
Crohn disease
435articles
435mentions
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 60Association of SLC22A4 and TNF-α gene polymorphism with susceptibility to inflammatory bowel disease among patients in the Eastern Province of Saudi Arabia.
PMID 41203454 | DOI 10.1016/j.ajg.2025.09.007 · Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology · 2025 · 12 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | Crohn disease | “Ulcerative Colitis (UC) and Crohn's Disease (CD) are the two main types of IBD.” | 0.93 | phenotype_alias_lexicon_v2 |
| variant | C4136A | “Genetic variants C1672T (SLC22A4), G-207C (SLC22A5) G113A, C4136A, 35delA (DLG5) and (rs1799964) TNF-α have been reported to have significant associations with the development of IBD in various populations.” | 0.82 | literature_variant_regex_v2 |
| gene | SLC22A4 | “Association of SLC22A4 and TNF-α gene polymorphism with susceptibility to inflammatory bowel disease among patients in the Eastern Province of Saudi Arabia.” | 0.98 | hgnc_dict_v1 |
| gene | SLC22A5 | “Genetic variants C1672T (SLC22A4), G-207C (SLC22A5) G113A, C4136A, 35delA (DLG5) and (rs1799964) TNF-α have been reported to have significant associations with the development of IBD in various populations.” | 0.98 | hgnc_dict_v1 |