17q12 Knowledge Basedeletion syndrome · static snapshot
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Source updated kidney and urinary tract 1 supporting source confidence 80% novelty 80%

Updated: 17q12 Recurrent Deletion Syndrome in Childhood

pmc changed: +3/-90 sentences since the previous capture.

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How this was derived

Version 2 captured 2026-11-14. Newly added text includes: “Background: The 17q12 recurrent deletion syndrome is a genomic disorder encompassing a 1.4 to 1.5 Mb region that includes the HNF1B gene, and it manifests with remarkable phenotypic variability. Background: The 17q12 recurrent deletion syndrome is a genomic disorder encompassing a 1.4 to 1.5 Mb region that includes the HNF1B gene, and it manifests with remarkable phenotypic variability. Disclaimer”

Generated 2026-11-14, last changed today. Dedup key update:244. 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)

17q12 Recurrent Deletion Syndrome in Childhood peer_reviewed · published 2026-11-14T01:37:14+00:00 · live page
Background: The 17q12 recurrent deletion syndrome is a genomic disorder encompassing a 1.4 to 1.5 Mb region that includes the HNF1B gene, and it manifests with remarkable phenotypic variability. Background: The 17q12 recurrent deletion syndrome is a genomic disorder encompassing a 1.4 to 1.5 Mb region that includes the HNF1B gene, and it manifests with remarkable phenotypic variability. Disclaimer

Supporting documents (1)

DocumentSourcePublishedSeenRelevance
17q12 Recurrent Deletion Syndrome in Childhood pmc 2025-01-01 yesterday 1.00