icd 10 cm code for nephrotic syndrome

What is the ICD 10 diagnosis code for?

The ICD-10-CM is a catalog of diagnosis codes used by medical professionals for medical coding and reporting in health care settings. The Centers for Medicare and Medicaid Services (CMS) maintain the catalog in the U.S. releasing yearly updates.

How serious is nephrotic syndrome?

What are the complications of nephrotic syndrome? Serious complications of nephrotic syndrome include kidney failure or end stage renal disease (ESRD). This requires short-term or long-term dialysis. Blood clots and infection are other complications. These happen due to the loss of protein in the urine (proteinuria).

What are some signs of nephrotic syndrome?

Nephrotic syndrome is a collection of symptoms due to kidney damage. This includes protein in the urine, low blood albumin levels, high blood lipids, and significant swelling. Other symptoms may include weight gain, feeling tired, and foamy urine. Complications may include blood clots, infections, and high blood pressure.

What does nephrotic syndrome stand for?

Nephrotic syndrome: pathophysiology and treatment.Nephrotic syndrome refers to the symptoms caused by renal injury in which large amounts of protein are lost in the urine. Common manifestations of the syndrome are proteinuria, edema, hypoalbuminemia, hyperlipidemia, and hypercoagulability.

What is nephrotic syndrome?

Patients usually show nephrotic syndrome indicating the presence of proteinuria with accompanying edema. A rare autosomal recessive inherited nephrotic syndrome that is present in the first week of life.

What is proteinuria in the kidney?

A condition characterized by severe proteinuria, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as hypoproteinemia; generalized edema; hypertension; and hyperlipidemias. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction. ...

What is nephrotic syndrome?

A kidney disease with no or minimal histological glomerular changes on light microscopy and with no immune deposits. It is characterized by lipid accumulation in the epithelial cells of kidney tubules and in the urine. Patients usually show nephrotic syndrome indicating the presence of proteinuria with accompanying edema.

What is autosomal recessive inherited nephrotic syndrome?

A rare autosomal recessive inherited nephrotic syndrome that is present in the first week of life. It manifests with edema and proteinuria and usually has a poor prognosis. Diseases involving defective kidney glomeruli, characterized by massive proteinuria and lipiduria with varying degrees of edema, hypoalbuminemia, and hyperlipidemia.

What is renal dysfunction?

A collection of symptoms that include severe edema, proteinuria, and hypoalbuminemia; it is indicative of renal dysfunction. A condition characterized by severe proteinuria, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as hypoproteinemia; generalized edema; hypertension;