17q12 Knowledge Basedeletion syndrome · static snapshot
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Phenotype expansion kidney and urinary tract 1 supporting source confidence 97% novelty 90%

New observation reported: We report a 5 year old, end stage kidney disease patient with renal cysts and hypertriglyceridemia (in the abs…

A source describes a new or expanded observation: “We report a 5 year old, end stage kidney disease patient with renal cysts and hypertriglyceridemia (in the absence of overt diabetes) with a known pathogenic mutation in the Hepatocyte Nuclear Factor-1β ( HNF-1β ) gene on chromosome 17q12.”

How this was derived

Flagged by novelty language (“for the first time”, “expands the phenotype”, …) in pmc.

Generated 2026-11-13, last changed today. Dedup key expansion:3c933d. 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)

We report a 5 year old, end stage kidney disease patient with renal cysts and hypertriglyceridemia (in the absence of overt diabetes) with a known pathogenic mutation in the Hepatocyte Nuclear Factor-1β ( HNF-1β ) gene on chromosome 17q12.

Supporting documents (1)

ArticleSourcePublishedSeenRelevance
A Boy with End-Stage Kidney Disease and Hypertriglyceridemia pmc 2024-01-01 yesterday 1.00