Q61.1 - Polycystic kidney, infantile type
- Applicable to Polycystic kidney, infantile type
- The 2025 edition of ICD10-CM Q61.1 became effective on October 1, 2024.
- This is the American ICD10-CM version of Q61.1 - other international versions of ICD10 Q61.1 may differ.
- Q61.1 is a Non-Billable / Non-Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- Q61.1 Code should not be used for billing or reimbursement purposes as there are multiple ICD-10 CM codes below it that contain a greater level of detail.
- Q61.1 - Polycystic kidney, infantile type
- Q61.1 - Polycystic kidney, infantile type
- Q61.11 - Cystic dilatation of collecting ducts
- Q61.19 - Other polycystic kidney, infantile type
Inclusion terms help to clarify and specify the conditions or diseases covered by a particular ICD-10-CM code.
Inclusion Term:
- Polycystic kidney, autosomal recessive
Non-Billable/Non-Specific Code
The following codes above Q61.1 contain annotation back-references that may be applicable to Q61.1:
- Chapter: Q00-Q99 - Congenital malformations, deformations and chromosomal abnormalities
- Section: Q60-Q64 - Congenital malformations of the urinary system
- Category: Q61 - Cystic kidney disease
Browse other similar CM codes:
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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