2020 ICD-10-CM Diagnosis Code Q60.5

Renal hypoplasia, unspecified

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
  • Q60.5 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2020 edition of ICD-10-CM Q60.5 became effective on October 1, 2019.
  • This is the American ICD-10-CM version of Q60.5 - other international versions of ICD-10 Q60.5 may differ.
The following code(s) above Q60.5 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 Q60.5:
  • Q00-Q99
    2020 ICD-10-CM Range Q00-Q99

    Congenital malformations, deformations and chromosomal abnormalities

    Note
    • Codes from this chapter are not for use on maternal records
    Type 2 Excludes
    • inborn errors of metabolism (E70-E88)
    Congenital malformations, deformations and chromosomal abnormalities
  • Q60
    ICD-10-CM Diagnosis Code Q60

    Renal agenesis and other reduction defects of kidney

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Includes
    • congenital absence of kidney
    • congenital atrophy of kidney
    • infantile atrophy of kidney
    Renal agenesis and other reduction defects of kidney
Approximate Synonyms
  • Congenital hypoplasia of kidney
  • Hypoplasia of kidney, congenital
  • Oligomeganephronia
  • Oligomeganephronic hypoplasia of kidney
Present On Admission
POA 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.
  • Q60.5 is considered exempt from POA reporting.
ICD-10-CM Q60.5 is grouped within Diagnostic Related Group(s) (MS-DRG v37.0):
  • 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 Q60.5 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

Diagnosis Index entries containing back-references to Q60.5:

ICD-10-CM Codes Adjacent To Q60.5
Q56.1 Male pseudohermaphroditism, not elsewhere classified
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
Q61.00 …… unspecified
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

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.