BETA v.3.0

2025 ICD-10-CM code Q61.00

Congenital renal cyst, unspecified.

This code should not be used for acquired renal cysts or when a more specific diagnosis of cystic kidney disease can be made. In case of uncertainty, further investigation is needed to classify into the correct subcategory.

Medical necessity for diagnostic testing and follow-up is determined by the size and location of the cyst, potential impact on kidney function, presence of associated anomalies, and family history of cystic kidney disease.

Diagnosis and management of this condition is typically overseen by a nephrologist or pediatrician specializing in kidney disorders.Further evaluation and intervention may depend on associated conditions and impact on renal function.

In simple words: A congenital renal cyst, unspecified, indicates the presence of a simple cyst found in the kidney at the time of birth. It is not acquired later in life and is not associated with more complex cystic kidney diseases.

A cyst present from birth affecting the kidney, not otherwise specified.

Example 1: A newborn infant undergoes a renal ultrasound that incidentally reveals a small, solitary cyst on the left kidney.Since it is present at birth and uncomplicated, the appropriate diagnosis code is Q61.00., During a fetal anomaly scan, a developing fetus is found to have multiple small cysts in both kidneys.In the absence of other associated anomalies or genetic syndromes, this could be coded as Q61.00 at birth., An infant with a family history of cystic kidney disease is evaluated and found to have a solitary renal cyst. As the type of cyst isn't otherwise specified but is congenital, Q61.00 is the correct code.

Documentation should include imaging reports (ultrasound, CT, MRI) confirming the presence and characteristics of the cyst, as well as any associated findings or family history suggestive of genetic cystic kidney diseases.The congenital nature of the cyst should be clearly established.

** Excludes1: acquired cyst of kidney (N28.1) and Potter's syndrome (Q60.6).This code is for use in the context of a congenital condition. It is not applicable to cysts that develop later in life due to other causes. Further evaluation might be required to rule out more complex or syndromic conditions, especially if multiple cysts or other anomalies are present.

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