2021 ICD-10-CM Code Q61.2
Polycystic kidney, adult type
Valid for Submission
Q61.2 is a billable diagnosis code used to specify a medical diagnosis of polycystic kidney, adult type. The code Q61.2 is valid during the fiscal year 2021 from October 01, 2020 through September 30, 2021 for the submission of HIPAA-covered transactions.
The ICD-10-CM code Q61.2 might also be used to specify conditions or terms like adult type polycystic kidney disease type 1, adult type polycystic kidney disease type 2, autosomal dominant polycystic kidney disease, autosomal dominant polycystic kidney disease, autosomal dominant polycystic kidney disease , autosomal dominant polycystic kidney disease, etc. The code is exempt from present on admission (POA) reporting for inpatient admissions to general acute care hospitals.
ICD-10: | Q61.2 |
Short Description: | Polycystic kidney, adult type |
Long Description: | Polycystic kidney, adult type |
Code Classification
Tabular List of Diseases and Injuries
The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code Q61.2:
Inclusion Terms
Inclusion TermsThese terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- Polycystic kidney, autosomal dominant
Index to Diseases and Injuries
The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code Q61.2 are found in the index:
- - Cyst (colloid) (mucous) (simple) (retention)
- - congenital NEC - Q89.8
- - kidney - Q61.00
- - more than one (multiple) - Q61.02
- - specified as polycystic - Q61.3
- - adult type - Q61.2
- - specified as polycystic - Q61.3
- - more than one (multiple) - Q61.02
- - kidney - Q61.00
- - kidney (acquired) - N28.1
- - congenital NEC - Q89.8
- - Cystic - See Also: condition;
- - kidney (congenital) - Q61.9
- - adult type - Q61.2
- - kidney (congenital) - Q61.9
- - Degeneration, degenerative
- - kidney - N28.89
- - polycystic - Q61.3
- - adult type (autosomal dominant) - Q61.2
- - polycystic - Q61.3
- - kidney - N28.89
- - Disease, diseased - See Also: Syndrome;
- - kidney (functional) (pelvis) - N28.9
- - polycystic - Q61.3
- - adult type - Q61.2
- - polycystic - Q61.3
- - polycystic
- - kidney or renal - Q61.3
- - adult type - Q61.2
- - kidney or renal - Q61.3
- - renal (functional) (pelvis) - See Also: Disease, kidney; - N28.9
- - polycystic (congenital) - Q61.3
- - adult type - Q61.2
- - polycystic (congenital) - Q61.3
- - kidney (functional) (pelvis) - N28.9
- - Nephritis, nephritic (albuminuric) (azotemic) (congenital) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic) - N05.9
- - polycystic - Q61.3
- - adult type - Q61.2
- - autosomal
- - dominant - Q61.2
- - polycystic - Q61.3
- - Polycystic (disease)
- - degeneration, kidney - Q61.3
- - autosomal dominant (adult type) - Q61.2
- - kidney - Q61.3
- - autosomal
- - dominant - Q61.2
- - autosomal dominant (adult type) - Q61.2
- - autosomal
- - degeneration, kidney - Q61.3
Approximate Synonyms
The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:
- Adult type polycystic kidney disease type 1
- Adult type polycystic kidney disease type 2
- Autosomal dominant polycystic kidney disease
- Autosomal dominant polycystic kidney disease
- Autosomal dominant polycystic kidney disease
- Autosomal dominant polycystic kidney disease
- Autosomal dominant polycystic kidney disease in childhood
- Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
- Tuberous sclerosis syndrome
Diagnostic Related Groups - MS-DRG Mapping
The ICD-10 code Q61.2 is grouped in the following groups for version MS-DRG V38.0 What are Diagnostic Related Groups?
The Diagnostic Related Groups (DRGs) are a patient classification scheme which provides a means of relating the type of patients a hospital treats. The DRGs divides all possible principal diagnoses into mutually exclusive principal diagnosis areas referred to as Major Diagnostic Categories (MDC). applicable from 10/01/2020 through 09/30/2021.
Present on Admission (POA)
Q61.2 is exempt from POA reporting - The Present on Admission (POA) indicator is used for diagnosis codes included in claims involving inpatient admissions to general acute care hospitals. POA indicators must be reported to CMS on each claim to facilitate the grouping of diagnoses codes into the proper Diagnostic Related Groups (DRG). CMS publishes a listing of specific diagnosis codes that are exempt from the POA reporting requirement. Review other POA exempt codes here .
CMS POA Indicator Options and Definitions
POA Indicator Code | POA Reason for Code | CMS will pay the CC/MCC DRG? |
---|---|---|
Y | Diagnosis was present at time of inpatient admission. | YES |
N | Diagnosis was not present at time of inpatient admission. | NO |
U | Documentation insufficient to determine if the condition was present at the time of inpatient admission. | NO |
W | Clinically undetermined - unable to clinically determine whether the condition was present at the time of inpatient admission. | YES |
1 | Unreported/Not used - Exempt from POA reporting. | NO |
Convert Q61.2 to ICD-9 Code
- 753.13 - Polycyst kid-autosom dom
Information for Patients
Kidney Cysts
A cyst is a fluid-filled sac. You may get simple kidney cysts as you age; they are usually harmless. There are also some diseases which cause kidney cysts. One type is polycystic kidney disease (PKD). It runs in families. In PKD, many cysts grow in the kidneys. This can enlarge the kidneys and make them work poorly. About half of people with the most common type of PKD end up with kidney failure. PKD also causes cysts in other parts of the body, such as the liver.
Often, there are no symptoms at first. Later, symptoms include
- Pain in the back and lower sides
- Headaches
- Blood in the urine
Doctors diagnose PKD with imaging tests and family history. There is no cure. Treatments can help with symptoms and complications. They include medicines and lifestyle changes, and if there is kidney failure, dialysis or kidney transplants.
Acquired cystic kidney disease (ACKD) happens in people who have chronic kidney disease, especially if they are on dialysis. Unlike PKD, the kidneys are normal sized, and cysts do not form in other parts of the body. ACKD often has no symptoms. Usually, the cysts are harmless and do not need treatment. If they do cause complications, treatments include medicines, draining the cysts, or surgery.
NIH: National Institute of Diabetes and Digestive and Kidney Diseases
- Acquired Cystic Kidney Disease - NIH (National Institute of Diabetes and Digestive and Kidney Diseases)
- Medullary cystic kidney disease (Medical Encyclopedia)
- Polycystic kidney disease (Medical Encyclopedia)
[Learn More]
Polycystic kidney disease Polycystic kidney disease is a disorder that affects the kidneys and other organs. Clusters of fluid-filled sacs, called cysts, develop in the kidneys and interfere with their ability to filter waste products from the blood. The growth of cysts causes the kidneys to become enlarged and can lead to kidney failure. Cysts may also develop in other organs, particularly the liver.Frequent complications of polycystic kidney disease include dangerously high blood pressure (hypertension), pain in the back or sides, blood in the urine (hematuria), recurrent urinary tract infections, kidney stones, and heart valve abnormalities. Additionally, people with polycystic kidney disease have an increased risk of an abnormal bulging (an aneurysm) in a large blood vessel called the aorta or in blood vessels at the base of the brain. Aneurysms can be life-threatening if they tear or rupture.The two major forms of polycystic kidney disease are distinguished by the usual age of onset and the pattern in which it is passed through families. The autosomal dominant form (sometimes called ADPKD) has signs and symptoms that typically begin in adulthood, although cysts in the kidney are often present from birth or childhood. Autosomal dominant polycystic kidney disease can be further divided into type 1 and type 2, depending on the genetic cause. The autosomal recessive form of polycystic kidney disease (sometimes called ARPKD) is much rarer and is often lethal early in life. The signs and symptoms of this condition are usually apparent at birth or in early infancy.
[Learn More]
Code History
- FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
- FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
- FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
- FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
- FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
- FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016 (First year ICD-10-CM implemented into the HIPAA code set)