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ALL MEDICAL CODES IN CATEGORY Congenital malformations of the urinary system
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 Q62.60
Malposition of the ureter, unspecified.
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 Q64.74
Double urethra.
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 Q61.11
Cystic dilatation of collecting ducts. This condition is a congenital malformation of the urinary system.
2025 ICD-10-CM code Q60.6
Potter's syndrome
2025 ICD-10-CM code Q61
Cystic kidney disease
2025 ICD-10-CM code Q61.0
Congenital renal cyst.A cyst present in the kidney at birth.
2025 ICD-10-CM code Q61.00
Congenital renal cyst, unspecified.
2025 ICD-10-CM code Q61.01
Congenital single renal cyst.
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 Q62.1
Congenital occlusion of the ureter.
2025 ICD-10-CM code Q62.8
Other congenital malformations of the ureter.
2025 ICD-10-CM code Q62.12
Congenital occlusion of the ureterovesical orifice.
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 Q64.75
Double urinary meatus is a congenital anomaly characterized by the presence of two external urethral openings.
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 Q64.39
Other atresia and stenosis of urethra and bladder neck.
2025 ICD-10-CM code Q61.02
Congenital multiple renal cysts.
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 Q62.5
Duplication of ureter. This is a congenital condition where an individual has two ureters on one side.
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 Q61.2
Polycystic kidney, adult type (also known as autosomal dominant polycystic kidney disease).
2025 ICD-10-CM code Q61.4
Renal dysplasia. Multicystic dysplastic kidney.
2025 ICD-10-CM code Q61.5
Medullary cystic kidney disease, including nephronophthisis and sponge kidney.
2025 ICD-10-CM code Q61.9
Cystic kidney disease, unspecified.
2025 ICD-10-CM code Q62
Congenital obstructive defects of the renal pelvis and congenital malformations of the ureter.
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 Q63.3
Hyperplastic and giant kidney; compensatory hypertrophy of the kidney.
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 Q64.0
Epispadias is a congenital defect where the urethra opens on the upper surface of the penis.
2025 ICD-10-CM code Q64.12
Cloacal exstrophy of the urinary bladder.
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 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 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 Q64.31
Congenital bladder neck obstruction. Congenital obstruction of vesicourethral orifice.
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 Q62.2
Congenital megaureter. Congenital dilatation of ureter.
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 Q62.39
Other obstructive defects of the renal pelvis and ureter.
2025 ICD-10-CM code Q60.1
Bilateral renal agenesis, a congenital absence of both kidneys.
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 Q62.61
Deviation of the ureter, a congenital anomaly.
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