Q60.6
BillablePotter's syndrome
Potter's syndrome
Status
Billable / Specific
Parent Code
Q60Coding Notes
Includes
Conditions included under this code
- congenital absence of kidney
- congenital atrophy of kidney
- infantile atrophy of kidney
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Potter facies24814002
- Potter's facies24814002
- BRA - Bilateral renal agenesis41962002
- Bilateral congenital absence of kidneys41962002
- Congenital absence of kidneys syndrome41962002
- Oligohydramnios sequence41962002
- Potter syndrome41962002
- Potter's anomaly of the kidney41962002
- Renal agenesis syndrome41962002
- Renofacial syndrome41962002
- Congenital absence of the kidney204942005
- Renal agenesis204942005
- Left kidney absent443768001
- Right kidney absent443806007
- Potter sequence cleft lip and palate cardiopathy syndrome716740009
- Thomas syndrome716740009
- Agenesis of left kidney762907005
- Left renal agenesis762907005
- Agenesis of right kidney762908000
- Right renal agenesis762908000
UMLS
- Oligohydramnios sequenceC0178426
- Oligohydramnios sequence (disorder)C0178426
- Potter SyndromeC0178426
- Potter sequenceC0178426
- Potter syndromeC0178426
- Potter's SequenceC0178426
- Potter's anomaly of the kidneyC0178426
- Potter's syndromeC0178426
- potter syndromeC0178426
- potter's syndromeC0178426
- potters syndromeC0178426
- syndrome potterC0178426
Frequently Asked Questions
What is the ICD-10 code for potter's syndrome?
The ICD-10-CM code for potter's syndrome is Q60.6. The full clinical description is "Potter's syndrome". Q60.6 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q60.6 mean?
ICD-10-CM code Q60.6 represents "Potter's syndrome". It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q60.6 a billable code?
Yes, Q60.6 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q60.6 in?
Q60.6 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q60.6 map to?
Q60.6 maps to 8 SNOMED CT concepts: 762907005, 762908000, 41962002, 204942005, 443768001, and 3 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q60.6?
Q60.6 is linked to 1 UMLS Concept Unique Identifier: C0178426. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.