ICD-10 Diagnosis Code Q61.5

Medullary cystic kidney

Diagnosis Code Q61.5

ICD-10: Q61.5
Short Description: Medullary cystic kidney
Long Description: Medullary cystic kidney
This is the 2017 version of the ICD-10-CM diagnosis code Q61.5

Valid for Submission
The code Q61.5 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Congenital malformations of the urinary system (Q60-Q64)
      • Cystic kidney disease (Q61)

Information for Medical Professionals

Diagnostic Related Groups
The diagnosis code Q61.5 is grouped in the following Diagnostic Related Group(s) (MS-DRG V34.0)

  • 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 to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

Present on Admission (POA) Additional informationCallout TooltipPresent on Admission
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.

The code Q61.5 is exempt from POA reporting.

Synonyms
  • Adolescent nephronophthisis
  • Congenital cystic kidney disease
  • Infantile nephronophthisis
  • Juvenile nephronophthisis
  • Medullary cystic disease
  • Medullary cystic disease, adult type
  • Medullary cystic kidney disease type 1
  • Medullary cystic kidney disease type 2
  • Medullary sponge kidney
  • Medullary sponge kidney with nephrocalcinosis
  • Medullary sponge kidney without nephrocalcinosis
  • Nephronophthisis
  • Nephronophthisis - medullary cystic disease
  • Nephronophthisis type 4
  • Nephronophthisis type 5
  • Nephronophthisis type 6

Index of Diseases and Injuries
References found for the code Q61.5 in the Index of Diseases and Injuries:


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)


[Read More]

Medullary cystic kidney disease type 1 Medullary cystic kidney disease type 1 (MCKD1) is an inherited condition that affects the kidneys. It leads to scarring (fibrosis) and impaired function of the kidneys, usually beginning in adulthood. The kidneys filter fluid and waste products from the body. They also reabsorb needed nutrients and release them back into the blood. As MCKD1 progresses, the kidneys are less able to function, resulting in kidney failure.Declining kidney function in people with MCKD1 leads to the signs and symptoms of the condition. The features are variable, even among members of the same family. Many individuals with MCKD1 develop high blood pressure (hypertension), especially as kidney function worsens. Some develop high levels of a waste product called uric acid in the blood (hyperuricemia) because the damaged kidneys are unable to remove uric acid effectively. In a small number of affected individuals, the buildup of this waste product can cause gout, which is a form of arthritis resulting from uric acid crystals in the joints.Although the condition is named medullary cystic kidney disease, only about 40 percent of affected individuals have medullary cysts, which are fluid filled pockets found in a particular region of the kidney. When present, the cysts are usually found in the inner part of the kidney (the medullary region) or the border between the inner and outer parts (corticomedullary region). These cysts are visible by tests such as ultrasound or CT scan.
[Read More]
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