17q12, explained for kidsdeletion syndrome · static snapshot
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A new article Kidneys and diabetes 1 supporting source confidence 97% novelty 75%

Genetics of CAKUT

Congenital anomalies of the kidney and urinary tract (CAKUT) represent a heterogeneous group of developmental disorders and are the leading cause of pediatric chronic kidney disease worldwide.

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How this was derived

Indexed from **pmc** on 2026-11-13 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-14, last changed today. Dedup key newdoc:189. 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)

Genetics of CAKUT peer_reviewed · published 2026-01-01 · live page
Below, we give several recent key examples how genetic discoveries have extended our understanding of human kidney (mal)development (Table 2): Novel monogenic discoveries ZMYM2 (chr13q12.11): De novo or inherited heterozygous loss-of-function variants cause syndromic CAKUT.

Supporting documents (1)

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Genetics of CAKUT pmc 2026-01-01 yesterday 1.00