Glomerular diseases N00-N08 >

 

Code Also

any associated kidney failure

Type 1 Excludes

hypertensive chronic kidney disease

 

Acute nephritic syndrome N00- >

 

Type 1 Excludes

acute tubulo-interstitial nephritis (N10)

nephritic syndrome NOS (N05.-)

Includes

acute glomerular disease

acute glomerulonephritis

acute nephritis

 

Rapidly progressive nephritic syndrome N01- >

 

Type 1 Excludes

nephritic syndrome NOS (N05.-)

Includes

rapidly progressive glomerular disease

rapidly progressive glomerulonephritis

rapidly progressive nephritis

 

Recurrent and persistent hematuria N02- >

 

Type 1 Excludes

acute cystitis with hematuria (N30.01)

hematuria NOS (R31.9)

hematuria not associated with specified morphologic lesions (R31.-)

 

Chronic nephritic syndrome N03- >

 

Type 1 Excludes

chronic tubulo-interstitial nephritis (N11.-)

diffuse sclerosing glomerulonephritis (N05.8-)

nephritic syndrome NOS (N05.-)

Includes

chronic glomerular disease

chronic glomerulonephritis

chronic nephritis

 

Nephrotic syndrome N04- >

 

Includes

congenital nephrotic syndrome

lipoid nephrosis

Clinical Information

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; and hyperlipidemias. Diseases

associated with nephrotic syndrome generally cause chronic kidney

dysfunction.

A kidney disease characterized by a high protein level in urine

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.

Nephrotic syndrome: twenty-four hour urine protein > three grams.

May be associated with hypoalbuminemia and hypercholesterolemia.

 

Type 1 Excludes

nephropathy NOS with no stated morphological lesion (N28.9)

renal disease NOS with no stated morphological lesion (N28.9)

tubulo-interstitial nephritis NOS (N12)

Includes

glomerular disease NOS

glomerulonephritis NOS

nephritis NOS

nephropathy NOS and renal disease NOS with morphological lesion

specified in .0-.8

Clinical Information

A renal disorder characterized by damage in the glomeruli. It may

be acute or chronic, focal or diffuse, and it may lead to renal

failure. Causes include autoimmune disorders, infections, diabetes,

and malignancies.

Glomerular disease characterized by an inflammatory reaction, with

leukocyte infiltration and cellular proliferation of the glomeruli,

or that appears to be the result of immune glomerular injury.

Inflammation of any part of the kidney.

Inflammation of the kidney. It is a focal or diffuse proliferative

or destructive process which may involve the glomerulus, tubule, or

interstitial renal tissue. (mesh)

Inflammation of the kidney; a focal or diffuse proliferative or

destructive process which may involve the glomerulus, tubule, or

interstitial renal tissue.

Inflammation of the renal glomeruli (kidney glomerulus) that can

be classified by the type of glomerular injuries including antibody

deposition, complement activation, cellular proliferation, and

glomerulosclerosis. These structural and functional abnormalities

usually lead to hematuria; proteinuria; hypertension; and renal

insufficiency.

 

Isolated proteinuria with specified morphological lesion N06- >

 

Type 1 Excludes

Proteinuria not associated with specific morphologic lesions (R80.0)

 

Hereditary nephropathy, not elsewhere classified N07- >

 

Type 2 Excludes

Alport's syndrome (Q87.81-)

hereditary amyloid nephropathy (E85.-)

nail patella syndrome (Q87.2)

non-neuropathic heredofamilial amyloidosis (E85.-)

 

Glomerular disorders in diseases classified elsewhere N08- >

 

Applicable To

Glomerulonephritis

Nephritis

Nephropathy

Code First

underlying disease, such as:

amyloidosis (E85.-)

congenital syphilis (A50.5)

cryoglobulinemia (D89.1)

disseminated intravascular coagulation (D65)

gout (M1A.-, M10.-)

microscopic polyangiitis (M31.7)

multiple myeloma (C90.0-)

sepsis (A40.0-A41.9)

sickle-cell disease (D57.0-D57.8)

Type 1 Excludes

glomerulonephritis, nephritis and nephropathy (in):

antiglomerular basement membrane disease (M31.0)

diabetes (E08-E13 with .21)

gonococcal (A54.21)

Goodpasture's syndrome (M31.0)

hemolytic-uremic syndrome (D59.3)

lupus (M32.14)

mumps (B26.83)

syphilis (A52.75)

systemic lupus erythematosus (M32.14)

Wegener's granulomatosis (M31.31)

pyelonephritis in diseases classified elsewhere (N16)

renal tubulo-interstitial disorders classified elsewhere (N16)

Clinical Information

A neoplastic or non-neoplastic condition affecting the kidney.

Representative examples of non-neoplastic conditions include

glomerulonephritis and nephrotic syndrome. Representative examples

of neoplastic conditions include benign processes (e.g., renal lipoma

and renal fibroma) and malignant processes (e.g., renal cell carcinoma

and renal lymphoma).

A renal disorder characterized by damage in the glomeruli. It may be

acute or chronic, focal or diffuse, and it may lead to renal failure.

Causes include autoimmune disorders, infections, diabetes, and

malignancies.

A term referring to any disease affecting the kidneys.

Glomerular disease characterized by an inflammatory reaction, with

leukocyte infiltration and cellular proliferation of the glomeruli,

or that appears to be the result of immune glomerular injury.

Impairment of health or a condition of abnormal functioning of the

kidney.

Inflammation of any part of the kidney.

Inflammation of the kidney. It is a focal or diffuse proliferative

or destructive process which may involve the glomerulus, tubule, or

interstitial renal tissue. (mesh)

Inflammation of the kidney; a focal or diffuse proliferative or

destructive process which may involve the glomerulus, tubule, or

interstitial renal tissue.

Inflammation of the renal glomeruli (kidney glomerulus) that can be

classified by the type of glomerular injuries including antibody

deposition, complement activation, cellular proliferation, and

glomerulosclerosis. These structural and functional abnormalities

usually lead to hematuria; proteinuria; hypertension; and renal

insufficiency.

Pathological processes of the kidney or its component tissues.

Your kidneys are two bean-shaped organs, each about the size of

your fists. They are located near the middle of your back, just

below the rib cage. Inside each kidney about a million tiny structures

called nephrons filter blood. They remove waste products and extra water,

which become urine. The urine flows through tubes called ureters 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 are at greater risk for 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 run tests to find out if you have kidney disease. If your

kidneys fail completely, a kidney transplant or dialysis can replace the

work your kidneys normally do.

 

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