Short description: Nephrotic syndrome w diffuse membranous glomerulonephritis. The 2021 edition of ICD-10-CM N04.2 became effective on October 1, 2020. This is the American ICD-10-CM version of N04.2 - other international versions of ICD-10 N04.2 may differ.
N04.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Nephrotic syndrome with unspecified morphologic changes 1 A collection of symptoms that include severe edema, proteinuria,... 2 A condition characterized by severe proteinuria, greater than 3.5 g/day in an average adult. 3 A kidney disease characterized by a high protein level in urine. 4 Diseases involving defective kidney glomeruli,...
Nephrotic syndrome with unspecified morphologic changes. N04.9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
MN is one of the most common causes of nephrotic syndrome. When your immune system attacks the glomeruli in membranous nephropathy, it causes changes to the filters that lead you to lose large amount of protein into the urine. If this continues at high levels, it can eventually lead to kidney failure.
ICD-10 code N04 for Nephrotic syndrome is a medical classification as listed by WHO under the range - Diseases of the genitourinary system .
The kidneys have filters that are responsible for cleaning waste products from your blood. In membranous nephropathy (MN), these filters are attacked by the body's immune system. Grouped together, the symptoms of this disease are called nephrotic syndrome.
Primary (autoimmune) disease accounts for at least 70% of membranous glomerulonephritis (MGN). The main causes of secondary MGN are lupus, hepatitis B, drugs, and malignancy. Other autoimmune or inflammatory diseases, and some infections, are associated with it less commonly.
Unspecified nephritic syndrome with diffuse membranous glomerulonephritis. N05. 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 N05.
ICD-10-CM Code for Nephrotic syndrome with diffuse membranous glomerulonephritis N04. 2.
Membranous nephropathy (MN), also known as membranous glomerulopathy, is one of the many glomerular diseases causing nephrotic syndrome. It is characterized by proteinuria, presenting with peripheral edema and frothy urine. The etiology can be primary or secondary.
Often, membranous nephropathy results from some type of autoimmune activity. Your body's immune system mistakes healthy tissue as foreign and attacks it with substances called autoantibodies. These autoantibodies target certain proteins located in the kidney's filtering systems (glomeruli).
Both nephritis and nephrosis are among the body's responses to injury or illness affecting the kidneys. Nephrotic syndrome is characterized by severe proteinuria, i.e. high amounts of protein, including albumin, in the urine, while nephritic syndrome's major feature is inflammation.
Membranoproliferative glomerulonephritis involves the basement membrane and mesangium, while membranous glomerulonephritis involves the basement membrane but not the mesangium. (Membranoproliferative glomerulonephritis has the alternate name "mesangiocapillary glomerulonephritis", to emphasize its mesangial character.)
Disease definition. A rare glomerular disease, histologically characterized by thickening of the capillary wall, with immune deposits predominantly containing IgG4 and C3 on the sub-epithelial side, and typically manifesting with nephrotic syndrome.
Membranous glomerulonephritis (MGN) is a specific type of GN. MGN develops when inflammation of your kidney structures causes problems with the functioning of your kidney. MGN is known by other names, including extramembranous glomerulonephritis, membranous nephropathy, and nephritis.
N04.A is a valid billable ICD-10 diagnosis code for Nephrotic syndrome with C3 glomerulonephritis . It is found in the 2021 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2020 - Sep 30, 2021 .
When an Excludes2 note appears under a code it is acceptable to use both the code and the excluded code together. A “code also” note instructs that two codes may be required to fully describe a condition, but this note does not provide sequencing direction. The sequencing depends on the circumstances of the encounter.
Congenital nephrotic syndrome is an inherited disorder characterized by protein in the urine and swelling of the body.
DRG Group #698-700 - Other kidney and urinary tract diagnoses with MCC.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code N04.2. Click on any term below to browse the alphabetical index.
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code N04.2 and a single ICD9 code, 581.1 is an approximate match for comparison and conversion purposes.