New publication
kidney and urinary tract
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.
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)
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)
| Document | Source | Published | Seen | Relevance |
|---|---|---|---|---|
| Genetics of CAKUT | pmc | 2026-01-01 | yesterday | 1.00 |