17q12 Knowledge Basedeletion syndrome · static snapshot
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Contradicting evidence kidney and urinary tract 1 supporting source confidence 97% novelty 70%

Caution: We report HNF1B screening in a cohort of 377 unrelated cases with various kidney phenotypes (hyperechogenic ki…

A source reports no association or a negative finding: “We report HNF1B screening in a cohort of 377 unrelated cases with various kidney phenotypes (hyperechogenic kidneys with size not more than +3 SD, multicystic kidney disease, renal agenesis, renal hypoplasia, cystic dysplasia, or hyperuricemic tubulointerstitial nephropathy not associated with UMOD ”

More contradicting evidence

How this was derived

Kept visible so the knowledge base does not only show positive results.

Generated 2026-11-13, last changed today. Dedup key negation:e2472c. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases. peer_reviewed · published 2010-06-01 · live page
We report HNF1B screening in a cohort of 377 unrelated cases with various kidney phenotypes (hyperechogenic kidneys with size not more than +3 SD, multicystic kidney disease, renal agenesis, renal hypoplasia, cystic dysplasia, or hyperuricemic tubulointerstitial nephropathy not associated with UMOD mutation).

Supporting documents (1)

ArticleSourcePublishedSeenRelevance
Spectrum of HNF1B mutations in a large cohort of patients who harbo... pubmed 2010-06-01 yesterday 1.00