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ALL MEDICAL CODES IN CATEGORY Congenital malformations of the urinary system

2025 ICD-10-CM code Q63.0

Accessory kidney is a congenital anomaly characterized by the presence of an extra kidney.

2025 ICD-10-CM code Q61.1

Polycystic kidney, infantile type.This code describes a rare, inherited kidney disorder characterized by multiple cysts in the kidneys.

2025 ICD-10-CM code Q61.19

Other polycystic kidney, infantile type. This code is used to classify a specific type of polycystic kidney disease in infants.

2025 ICD-10-CM code Q64.0

Epispadias is a congenital defect where the urethra opens on the upper surface of the penis.

2025 ICD-10-CM code Q62.60

Malposition of the ureter, unspecified.

2025 ICD-10-CM code Q60.1

Bilateral renal agenesis, a congenital absence of both kidneys.

2025 ICD-10-CM code Q64.75

Double urinary meatus is a congenital anomaly characterized by the presence of two external urethral openings.

2025 ICD-10-CM code Q64.12

Cloacal exstrophy of the urinary bladder.

2025 ICD-10-CM code Q64.32

Congenital stricture of the urethra.

2025 ICD-10-CM code Q62.10

Congenital occlusion of the ureter, unspecified.

2025 ICD-10-CM code Q61.4

Renal dysplasia. Multicystic dysplastic kidney.

2025 ICD-10-CM code Q64.11

Supravesical fissure of urinary bladder. This is a congenital defect where the bladder doesn't fully close at the top.

2025 ICD-10-CM code Q61.3

Polycystic kidney, unspecified.

2025 ICD-10-CM code Q63.1

This code represents a congenital malformation where the kidneys are lobulated, fused together, or shaped like a horseshoe.

2025 ICD-10-CM code Q61.0

Congenital renal cyst.A cyst present in the kidney at birth.

2025 ICD-10-CM code Q62.32

This code represents a cecoureterocele, which is a congenital anomaly where the ureter inserts into the bladder along with a portion of the kidney (renal tissue).

2025 ICD-10-CM code Q64.74

Double urethra.

2025 ICD-10-CM code Q62.11

Congenital occlusion of ureteropelvic junction. This is a blockage where the kidney and ureter connect.

2025 ICD-10-CM code Q62.5

Duplication of ureter. This is a congenital condition where an individual has two ureters on one side.

2025 ICD-10-CM code Q62.2

Congenital megaureter. Congenital dilatation of ureter.

2025 ICD-10-CM code Q64.31

Congenital bladder neck obstruction. Congenital obstruction of vesicourethral orifice.

2025 ICD-10-CM code Q64.6

Congenital diverticulum of bladder. This is a birth defect where an extra pouch or cavity forms in the bladder wall.

2025 ICD-10-CM code Q62.63

Anomalous implantation of ureter.

2025 ICD-10-CM code Q61

Cystic kidney disease

2025 ICD-10-CM code Q62.3

Other obstructive defects of renal pelvis and ureter. This condition describes congenital anomalies causing blockage of urine flow from the kidney to the bladder.

2025 ICD-10-CM code Q61.00

Congenital renal cyst, unspecified.

2025 ICD-10-CM code Q62.39

Other obstructive defects of the renal pelvis and ureter.

2025 ICD-10-CM code Q62.0

Congenital hydronephrosis is a condition where there is an abnormal widening of the renal pelvis and calyces of one or both kidneys, present at birth.

2025 ICD-10-CM code Q60.3

Renal hypoplasia, unilateral, affecting only one kidney.

2025 ICD-10-CM code Q62.12

Congenital occlusion of the ureterovesical orifice.

2025 ICD-10-CM code Q62.61

Deviation of the ureter, a congenital anomaly.

2025 ICD-10-CM code Q64.7

Other and unspecified congenital malformations of the bladder and urethra.

2025 ICD-10-CM code Q61.9

Cystic kidney disease, unspecified.

2025 ICD-10-CM code Q64.39

Other atresia and stenosis of urethra and bladder neck.

2025 ICD-10-CM code Q61.2

Polycystic kidney, adult type (also known as autosomal dominant polycystic kidney disease).

2025 ICD-10-CM code Q63

Other congenital malformations of kidney

2025 ICD-10-CM code Q61.02

Congenital multiple renal cysts.

2025 ICD-10-CM code Q63.8

Other specified congenital malformations of kidney. Congenital renal calculi.

2025 ICD-10-CM code Q63.9

Congenital malformation of kidney, unspecified.

2025 ICD-10-CM code Q64.2

Congenital posterior urethral valves. This is a developmental abnormality in male newborns where a membrane obstructs the posterior urethra, causing bladder obstruction.

2025 ICD-10-CM code Q61.11

Cystic dilatation of collecting ducts. This condition is a congenital malformation of the urinary system.

2025 ICD-10-CM code Q60.4

Renal hypoplasia, bilateral. This is a congenital condition characterized by underdevelopment of both kidneys.

2025 ICD-10-CM code Q64.3

Other atresia and stenosis of urethra and bladder neck. This condition involves a blockage or narrowing in the urethra and the opening of the bladder.

2025 ICD-10-CM code Q64.33

Congenital stricture of the urinary meatus.

2025 ICD-10-CM code Q64.10

Exstrophy of the urinary bladder, unspecified.Also known as ectopia vesicae.

2025 ICD-10-CM code Q64.19

Other exstrophy of the urinary bladder; a birth defect where the bladder is malformed, exposed, and protrudes through the abdominal wall.

2025 ICD-10-CM code Q60.5

Renal hypoplasia, unspecified: One or both kidneys are smaller than normal due to incomplete development.

2025 ICD-10-CM code Q64.70

Unspecified congenital malformation of the bladder and urethra.

2025 ICD-10-CM code Q64.71

Congenital prolapse of the urethra.

2025 ICD-10-CM code Q62.69

Other malposition of the ureter, a congenital anomaly.

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