ICD-10 Diagnosis Code N06.6

Isolated proteinuria with dense deposit disease

Diagnosis Code N06.6

ICD-10: N06.6
Short Description: Isolated proteinuria with dense deposit disease
Long Description: Isolated proteinuria with dense deposit disease
This is the 2018 version of the ICD-10-CM diagnosis code N06.6

Valid for Submission
The code N06.6 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Diseases of the genitourinary system (N00–N99)
    • Glomerular diseases (N00-N08)
      • Isolated proteinuria with specified morphological lesion (N06)

Information for Medical Professionals

Diagnostic Related Groups
The diagnosis code N06.6 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

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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.

Synonyms
  • Isolated proteinuria with specified morphological lesion, dense deposit disease

Index of Diseases and Injuries
References found for the code N06.6 in the Index of Diseases and Injuries:


Information for Patients


Kidney Diseases

Also called: Renal disease

You have two kidneys, each about the size of your fist. They are near the middle of your back, just below the rib cage. Inside each kidney there are about a million tiny structures called nephrons. They filter your blood. They remove wastes and extra water, which become urine. The urine flows through tubes called ureters. It goes to your bladder, which stores the urine until you go to the bathroom.

Most kidney diseases attack the nephrons. This damage may leave kidneys unable to remove wastes. Causes can include genetic problems, injuries, or medicines. You have a higher risk of kidney disease if you have diabetes, high blood pressure, or a close family member with kidney disease. Chronic kidney disease damages the nephrons slowly over several years. Other kidney problems include

  • Cancer
  • Cysts
  • Stones
  • Infections

Your doctor can do blood and urine tests to check if you have kidney disease. If your kidneys fail, you will need dialysis or a kidney transplant.

NIH: National Institute of Diabetes and Digestive and Kidney Diseases

  • ACE inhibitors (Medical Encyclopedia)
  • Acute nephritic syndrome (Medical Encyclopedia)
  • Analgesic nephropathy (Medical Encyclopedia)
  • Atheroembolic renal disease (Medical Encyclopedia)
  • Bartter syndrome (Medical Encyclopedia)
  • Bilateral hydronephrosis (Medical Encyclopedia)
  • Congenital nephrotic syndrome (Medical Encyclopedia)
  • Distal renal tubular acidosis (Medical Encyclopedia)
  • Focal segmental glomerulosclerosis (Medical Encyclopedia)
  • Glomerulonephritis (Medical Encyclopedia)
  • Goodpasture syndrome (Medical Encyclopedia)
  • IgA nephropathy (Medical Encyclopedia)
  • Injury - kidney and ureter (Medical Encyclopedia)
  • Interstitial nephritis (Medical Encyclopedia)
  • Kidney removal (Medical Encyclopedia)
  • Kidney removal - discharge (Medical Encyclopedia)
  • Medicines and Kidney Disease - NIH (National Kidney Disease Education Program)
  • Membranoproliferative GN I (Medical Encyclopedia)
  • Membranous nephropathy (Medical Encyclopedia)
  • Minimal change disease (Medical Encyclopedia)
  • Nephrocalcinosis (Medical Encyclopedia)
  • Nephrotic syndrome (Medical Encyclopedia)
  • Obstructive uropathy (Medical Encyclopedia)
  • Perirenal abscess (Medical Encyclopedia)
  • Proximal renal tubular acidosis (Medical Encyclopedia)
  • Reflux nephropathy (Medical Encyclopedia)
  • Renal papillary necrosis (Medical Encyclopedia)
  • Renal perfusion scintiscan (Medical Encyclopedia)
  • Renal vein thrombosis (Medical Encyclopedia)
  • Unilateral hydronephrosis (Medical Encyclopedia)


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Urine and Urination

Your kidneys make urine by filtering wastes and extra water from your blood. The waste is called urea. Your blood carries it to the kidneys. From the kidneys, urine travels down two thin tubes called ureters to the bladder. The bladder stores urine until you are ready to urinate. It swells into a round shape when it is full and gets smaller when empty. If your urinary system is healthy, your bladder can hold up to 16 ounces (2 cups) of urine comfortably for 2 to 5 hours.

You may have problems with urination if you have

  • Kidney failure
  • Urinary tract infections
  • An enlarged prostate
  • Bladder control problems like incontinence, overactive bladder, or interstitial cystitis
  • A blockage that prevents you from emptying your bladder

Some conditions may also cause you to have blood or protein in your urine. If you have a urinary problem, see your health care provider. Urinalysis and other urine tests can help to diagnose the problem. Treatment depends on the cause.

NIH: National Institute of Diabetes and Digestive and Kidney Diseases

  • Clean catch urine sample (Medical Encyclopedia)
  • Frequent or urgent urination (Medical Encyclopedia)
  • RBC urine test (Medical Encyclopedia)
  • Urinalysis (Medical Encyclopedia)
  • Urinary catheters (Medical Encyclopedia)
  • Urinary Retention - NIH (National Institute of Diabetes and Digestive and Kidney Diseases)
  • Urinating more at night (Medical Encyclopedia)
  • Urination - difficulty with flow (Medical Encyclopedia)
  • Urination - painful (Medical Encyclopedia)
  • Urine - bloody (Medical Encyclopedia)
  • Urine 24-hour volume (Medical Encyclopedia)
  • Urine odor (Medical Encyclopedia)


[Read More]

C3 glomerulopathy C3 glomerulopathy is a group of related conditions that cause the kidneys to malfunction. The major features of C3 glomerulopathy include high levels of protein in the urine (proteinuria), blood in the urine (hematuria), reduced amounts of urine, low levels of protein in the blood, and swelling in many areas of the body. Affected individuals may have particularly low levels of a protein called complement component 3 (or C3) in the blood.The kidney problems associated with C3 glomerulopathy tend to worsen over time. About half of affected individuals develop end-stage renal disease (ESRD) within 10 years after their diagnosis. ESRD is a life-threatening condition that prevents the kidneys from filtering fluids and waste products from the body effectively.Researchers have identified two major forms of C3 glomerulopathy: dense deposit disease and C3 glomerulonephritis. Although the two disorders cause similar kidney problems, the features of dense deposit disease tend to appear earlier than those of C3 glomerulonephritis, usually in adolescence. However, the signs and symptoms of either disease may not begin until adulthood.One of the two forms of C3 glomerulopathy, dense deposit disease, can also be associated with other conditions unrelated to kidney function. For example, people with dense deposit disease may have acquired partial lipodystrophy, a condition characterized by a lack of fatty (adipose) tissue under the skin in the upper part of the body. Additionally, some people with dense deposit disease develop a buildup of yellowish deposits called drusen in the light-sensitive tissue at the back of the eye (the retina). These deposits usually appear in childhood or adolescence and can cause vision problems later in life.
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