Q61.19
BillableOther polycystic kidney, infantile type
Other polycystic kidney, infantile type
Status
Billable / Specific
Parent Code
Q61.1Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(1)
Also Known As / Clinical Terms(13)
SNOMED CT
- ARPKD - Autosomal recessive polycystic kidney disease28770003
- Autosomal recessive infantile polycystic kidney disease28770003
- Autosomal recessive polycystic kidney disease28770003
- IPKD - Infantile polycystic kidney disease28770003
- Infantile polycystic kidney disease28770003
- Polycystic kidney disease, infantile type28770003
Clinical Terms
- Autosomal recessive infantile polycystic kidney disease
- Autosomal recessive polycystic kidney disease
- IPKD - Infantile polycystic kidney disease
- Polycystic kidney disease, infantile type
- ARPKD - Autosomal recessive polycystic kidney disease
- Infantile polycystic kidney disease
Frequently Asked Questions
What is the ICD-10 code for other polycystic kidney, infantile type?
The ICD-10-CM code for other polycystic kidney, infantile type is Q61.19. The full clinical description is "Other polycystic kidney, infantile type". Q61.19 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q61.19 mean?
ICD-10-CM code Q61.19 represents “Other polycystic kidney, infantile type”. 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 Q61.19 a billable code?
Yes, Q61.19 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q61.19 in?
Q61.19 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q61.19?
Q61.19 has Excludes1 notes indicating codes that cannot be used together with it, including: acquired cyst of kidney (N28.1); Potter's syndrome (Q60.6).
What SNOMED CT codes does Q61.19 map to?
Q61.19 maps to 1 SNOMED CT concept: 28770003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q61.19?
Q61.19 is linked to 1 UMLS Concept Unique Identifier: C2910225. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q61.19 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other polycystic kidney, infantile type affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q61.19?
There is no direct ICD-11 mapping available for Q61.19 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.