17q12 Knowledge Basedeletion syndrome · static snapshot
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Frequency / statistic Research frontier 1 supporting source confidence 97% novelty 60%

HNF1B mutation-related MODY5 DM has been reported in 63% of patients with 17q12 deletion syndrome ( 9 )

A source reports “63%” in the context of general: “HNF1B mutation-related MODY5 DM has been reported in 63% of patients with 17q12 deletion syndrome ( 9 ).”

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How this was derived

Numbers are quoted verbatim from the source; check the source before quoting onward.

Generated 2026-11-13, last changed yesterday. Dedup key freq:63%. 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)

A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deletion Syndrome peer_reviewed · published 2024-01-01 · live page
HNF1B mutation-related MODY5 DM has been reported in 63% of patients with 17q12 deletion syndrome ( 9 ).

Supporting documents (1)

DocumentSourcePublishedSeenRelevance
A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deleti... pmc 2024-01-01 yesterday 1.00