Congenital diverticulum of urinary bladder

Description

A condition caused by failure of the bladder to correctly develop. This condition is characterised by weakness in the bladder wall through which some of the lining of the bladder protrudes. This condition may present with urinary tract infections, difficulty voiding, or abdominal fullness. This condition may also be asymptomatic.

Index terms

Congenital diverticulum of urinary bladder
Hutch-diverticulum
congenital bladder diverticulum

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congenital vesical diverticulum

Exclusions from above levels

http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

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

Foundation entity

Congenital diverticulum of urinary bladder – http://id.who.int/icd/entity/17481526

Part of: LB31: Structural developmental anomalies of urinary tract › 20: Developmental anomalies