ICD-10-CM 274.11 - Uric acid nephrolithiasis Code 274.11 - Uric acid nephrolithiasis ⑨ [Outdated] There's more to see -- the rest of this entry is available only to subscribers. 274.11 - Uric acid nephrolithiasis Code Map to ⑩
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.
Use the code for a term followed by "NOS" when:
ICD-10 code R68. 89 for Other general symptoms and signs is a medical classification as listed by WHO under the range - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified .
Nephrotic syndrome is a kidney disorder that causes your body to pass too much protein in your urine. Nephrotic syndrome is usually caused by damage to the clusters of small blood vessels in your kidneys that filter waste and excess water from your blood.
2: Calculus of kidney with calculus of ureter.
Nephrotic syndrome is a condition that causes the kidneys to leak large amounts of protein into the urine. This can lead to a range of problems, including swelling of body tissues and a greater chance of catching infections.
Nephrosis is also called nephrotic syndrome, and is caused by a variety of diseases. These attacks on your body lead to your kidneys being unable to prevent proteins from leaking into your urine. Nephrosis is a condition that describes multiple symptoms which indicate your kidneys are not working like they should.
Nephrotic syndrome is not a specific kidney disease. It can occur in any kidney disease that damages the filtering units in a certain way that allows them to leak protein into the urine. Some of the diseases that cause nephrotic syndrome, such as nephritis, affect only the kidney.
The ureteropelvic junction is located where the pelvis of the kidney meets the ureter (the tube that drains urine into the bladder). The term ureteropelvic junction (UPJ) obstruction describes a blockage to this area.
2 for Hydronephrosis with renal and ureteral calculous obstruction is a medical classification as listed by WHO under the range - Diseases of the genitourinary system .
Hydronephrosis with renal and ureteral calculous obstruction N13. 2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM N13. 2 became effective on October 1, 2021.
Nephrotic syndrome (NS) is one of the commonest kidney diseases seen in childhood and is characterized by a relapsing remitting course. Various complications have been reported in children with NS, including infections, thromboembolism, hypovolemia, and acute kidney injury (AKI).
Nephritis (kidney inflammation) is most often caused by autoimmune diseases that affect major organs, although it can also result from infection. Nephritis can cause excessive amounts of protein to be excreted in urine, and fluid to build up in the body.
Secondary nephrotic syndrome Examples include IgA vasculitis (also known as Henoch-Schönlein purpura) and lupus. infections, including hepatitis B and C, HIV link, and malaria link. diseases of the blood, such as leukemia link, lymphoma link, and sickle cell disease link.
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.
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.
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;
The 2022 edition of ICD-10-CM N28.9 became effective on October 1, 2021.
A term referring to any disease affecting the kidneys. Conditions in which the function of kidneys deteriorates suddenly in a matter of days or even hours. It is characterized by the sudden drop in glomerular filtration rate. Impairment of health or a condition of abnormal functioning of the kidney.
The 2022 edition of ICD-10-CM N12 became effective on October 1, 2021.
For primary inflammation of glomerular interstitium, see glomerulonephritis . Infiltration of the inflammatory cells into the interstitial compartment results in edema, increased spaces between the tubules, and tubular renal dysfunction.
Inflammation of the kidney and its pelvis due to infection.
Clinical Information. A disorder characterized by an infectious process involving the kidney. An acute or chronic inflammatory process affecting the kidney. It is caused by bacteria and in most cases it is the result of a urinary tract infection.
Inflammation of the kidney pelvis and kidney calices where urine is collected before discharge, but does not involve the renal parenchyma (the nephrons) where urine is processed.