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Structural developmental anomalies of urinary tract

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Any condition caused by failure of the urinary tract to correctly develop during the antenatal period.

code elsewhere

• Allantoic duct remnants or cysts  (LB03.0)
• Persistent urogenital sinus  (LB42.Y)

sections/codes in this section (LB31-LB31)

• Congenital hydronephrosis  (LB31.0)
• Congenital primary megaureter  (LB31.1)
• Fetal lower urinary tract obstruction  (LB31.2)
• Exstrophy of urinary bladder  (LB31.3)
• Congenital diverticulum of urinary bladder  (LB31.4)
• Duplication of urethra  (LB31.5)
• Congenital megalourethra  (LB31.6)
• Megacystis-megaureter  (LB31.7)
• Atresia or stenosis of ureter  (LB31.8)
• Agenesis of ureter  (LB31.9)
• Duplication of ureter  (LB31.A)
• Malposition of ureter  (LB31.B)
• Congenital absence of bladder or urethra  (LB31.C)
• Congenital vesico-uretero-renal reflux  (LB31.D)
• Other specified structural developmental anomalies of urinary tract  (LB31.Y)
• Structural developmental anomalies of urinary tract, unspecified  (LB31.Z)

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