LB31.DICD-11 MMS 2026-01
Congenital vesico-uretero-renal reflux
Description
A condition caused by failure of the ureter to develop correctly during the antenatal period. This condition may present with urinary tract infection, or may be asymptomatic.
Index terms
- Congenital vesico-uretero-renal reflux
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
LB31.0– Congenital hydronephrosisLB31.1– Congenital primary megaureterLB31.2– Fetal lower urinary tract obstructionLB31.3– Exstrophy of urinary bladderLB31.4– Congenital diverticulum of urinary bladderLB31.5– Duplication of urethraLB31.6– Congenital megalourethraLB31.7– Megacystis-megaureterLB31.8– Atresia or stenosis of ureterLB31.9– Agenesis of ureterLB31.A– Duplication of ureterLB31.B– Malposition of ureterLB31.C– Congenital absence of bladder or urethraLB31.Y– Other specified structural developmental anomalies of urinary tractLB31.Z– Structural developmental anomalies of urinary tract, unspecified
Foundation entity
Congenital vesico-uretero-renal reflux – http://id.who.int/icd/entity/1136708449
Allowed postcoordination axes
Part of: LB31: Structural developmental anomalies of urinary tract › 20: Developmental anomalies