Fetal lower urinary tract obstruction

Description

A disease caused by partial or complete obstruction of the urethra, during the antenatal period. This disease can present with enlarged bladder, oligohydramnios, or pulmonary hypoplasia. Confirmation is through observation of the obstruction by imaging.

Index terms

Fetal lower urinary tract obstruction
Fetal LUTO - [lower urinary tract obstruction]
other atresia or stenosis of urethra or bladder neck

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Fetal lower urinary tract obstruction due to atresia of urethra
Congenital stricture of urethra
Congenital urethral atresia
congenital obstruction of urethra
Fetal lower urinary tract obstruction due to posterior urethral valve
PUV - [posterior urethral valve]
congenital posterior urethral valve
congenital urethral posterior valvular stricture
congenital urethral valve
posterior urethral valve
urethral valve formation
Fetal lower urinary tract obstruction due to anterior urethral valve
congenital anterior urethral valves
Congenital obstruction of bladder neck
congenital bladder neck stenosis
Atresia of vesicourethral orifice
imperforate urethra
Atresia of bladder
Atresia of bladder neck
Congenital stenosis of urethral valve
congenital urethral valvular stricture
congenital valvular stricture of urethra
Congenital urethral occlusion
Impervious urethra
congenital stenosis of urethra
congenital urethral stenosis
ostium ureteris stenosis
Congenital urinary meatus stricture
congenital meatal stenosis
congenital urinarius meatus stricture
congenital vesicourethral orifice stricture
stenosis of vesicourethral orifice
Obstructive congenital vesical hernia
Obstructive paraurethral ducts anomaly
Congenital pinhole urinary meatus
Obstructive bladder anomaly

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
LB31.3 – Exstrophy of urinary bladder
LB31.4 – Congenital diverticulum 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

Fetal lower urinary tract obstruction – http://id.who.int/icd/entity/1661120971

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