Diagnosis Code N28.1
Information for Medical Professionals
The diagnosis code N28.1 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 General 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.
- 593.2 - Cyst of kidney, acquired
- Acquired complex renal cyst
- Acquired polycystic kidney disease
- Acquired renal cyst with neoplastic change
- Acquired renal cyst without neoplastic change
- Acquired renal cystic disease
- Complex cyst of kidney
- Diabetes mellitus associated with genetic syndrome
- Hydatid cyst of kidney
- Infected renal cyst
- Multiple acquired kidney cysts
- Multiple renal cysts
- Parapelvic renal cyst
- Renal cysts and diabetes syndrome
- Rupture of kidney
- Ruptured cyst of kidney
- Simple renal cyst
- Single acquired kidney cyst
Index of Diseases and Injuries
References found for the code N28.1 in the Index of Diseases and Injuries:
- Inclusion Terms: Inclusion terms
List of terms is included under some codes. These 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.
- Cyst (multiple)(solitary) of kidney, acquired
- Type 1 Excludes Notes: Type 1 Excludes Notes
A type 1 Excludes note is a pure excludes note. It means “NOT CODED HERE!” An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- cystic kidney disease (congenital) (Q61.-)
Information for Patients
A cyst is a fluid-filled sac. There are two types of kidney cysts.
Polycystic kidney disease (PKD) runs in families. In PKD, the cysts take the place of the normal tissue. They enlarge the kidneys and make them work poorly, leading to kidney failure. When PKD causes kidneys to fail - which usually happens after many years - people need dialysis or kidney transplantation. 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.
Symptoms of PKD include
- Pain in the back and lower sides
- Urinary tract infections
- Blood in the urine
Doctors diagnose PKD with imaging tests and family history. Treatments include medications, and, when people with PKD develop kidney failure, dialysis or kidney transplants.
Acquired cystic kidney disease (ACKD) usually happens in people who are on dialysis. Unlike PKD, the kidneys are normal sized, and cysts do not form in other parts of the body. People with ACKD already have chronic kidney disease when they develop cysts. ACKD often has no symptoms. In most cases, the cysts are harmless and do not need treatment.
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
- Polycystic kidney disease