Template:ICD-11 Renal anomalies header table

ICD-11 Structural developmental anomalies of the urinary system

LB30 Structural developmental anomalies of kidneys - LB30.0 Renal agenesis or other reduction defects of kidney | LB30.1 Renal dysplasia | LB30.2 Congenital single renal cyst | LB30.3 Renal tubular dysgenesis | LB30.4 Oligomeganephronia | LB30.5 Accessory kidney | LB30.6 Fusion anomaly of kidneys | LB30.7 Ectopic or pelvic kidney | LB30.8 Medullary sponge kidney | LB30.9 Multicystic renal dysplasia LB31 Structural developmental anomalies of urinary tract - LB31.0 Congenital hydronephrosis | LB31.1 Congenital primary megaureter | LB31.2 Foetal lower urinary tract obstruction | 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 KC01 Congenital renal failure A severe irreversible decline in the ability of kidneys to remove wastes, concentrate urine, and maintain electrolyte balance; blood pressure; and calcium metabolism which existed at, or often before, birth.