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ICD-10-CM Codes
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Q00-Q99
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Q60-Q64
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2023 ICD-10-CM Diagnosis Code Q60.6
2023 ICD-10-CM Diagnosis Code Q60.6
Potter's syndrome
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt
- Q60.6 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM Q60.6 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q60.6 - other international versions of ICD-10 Q60.6 may differ.
The following code(s) above
Q60.6 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
Q60.6:
- Oligohydramnios sequence
- Potter syndrome
Clinical Information
- A rare, lethal congenital malformation characterized by bilateral renal agenesis and the absence or decreased volume of amniotic fluid (oligohydramnios). The presence of oligohydramnios gives rise to congenital anomalies that include hypoplastic lungs, lower extremities abnormalities, and characteristic facial features (low-set ears, widely separated eyes, nose flattening, and receding chin). Newborn infants usually die of respiratory failure.
Present On AdmissionPOA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
- Q60.6 is considered exempt from POA reporting.
ICD-10-CM Q60.6 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 698 Other kidney and urinary tract diagnoses with mcc
- 699 Other kidney and urinary tract diagnoses with cc
- 700 Other kidney and urinary tract diagnoses without cc/mcc
Convert Q60.6 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
Code annotations containing back-references to Q60.6:
- Potter's
- facies Q60.6
- syndrome Q60.6 (with renal agenesis)
ICD-10-CM Codes Adjacent To Q60.6
Q56.2 Female pseudohermaphroditism, not elsewhere classified
Q56.3 Pseudohermaphroditism, unspecified
Q56.4 Indeterminate sex, unspecified
Q60 Renal agenesis and other reduction defects of kidney
Q60.0 Renal agenesis, unilateral
Q60.1 Renal agenesis, bilateral
Q60.2 Renal agenesis, unspecified
Q60.3 Renal hypoplasia, unilateral
Q60.4 Renal hypoplasia, bilateral
Q60.5 Renal hypoplasia, unspecified
Q60.6
Potter's syndrome
Q61 Cystic kidney disease
Q61.0 Congenital renal cyst
Q61.01 Congenital single renal cyst
Q61.02 Congenital multiple renal cysts
Q61.1 Polycystic kidney, infantile type
Q61.11 Cystic dilatation of collecting ducts
Q61.19 Other polycystic kidney, infantile type
Q61.2 Polycystic kidney, adult type
Q61.3 Polycystic kidney, unspecified
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
