Q60.6

Potter's syndrome

Billable / specificPOA exempt

Q60.6 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Inclusion terms

Includes (from Q60)

  • congenital absence of kidney
  • congenital atrophy of kidney
  • infantile atrophy of kidney
  • Note: Codes from this chapter are not for use on maternal records

Excludes2

Not included here — may be reported together when both conditions exist.

  • inborn errors of metabolism (E70-E88) (from Q60)

Also known as

  • Potter's, facies
  • Potter's, syndrome

Parent code

  • Q60Renal agenesis and other reduction defects of kidneyHeader

Related codes

  • Q60.0Renal agenesis, unilateralBillable
  • Q60.1Renal agenesis, bilateralBillable
  • Q60.2Renal agenesis, unspecifiedBillable
  • Q60.3Renal hypoplasia, unilateralBillable
  • Q60.4Renal hypoplasia, bilateralBillable
  • Q60.5Renal hypoplasia, unspecifiedBillable

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