Glomerulonephritis

"Glomerulonephritis" References in the ICD-10-CM Index to Diseases and Injuries

References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "glomerulonephritis"

  • Glomerulonephritis - See Also: Nephritis; - N05.9 Unspecified nephritic syndrome with unspecified morphologic changes
    • acute - N00.9 Acute nephritic syndrome with unspecified morphologic changes
    • chronic - N03.9 Chronic nephritic syndrome with unspecified morphologic changes
    • crescentic (diffuse) NEC - See Also: N00-N07 with fourth character .7; - N05.7 Unspecified nephritic syndrome with diffuse crescentic glomerulonephritis
    • dense deposit - See Also: N00-N07 with fourth character .6; - N05.6 Unspecified nephritic syndrome with dense deposit disease
    • diffuse
      • crescentic - See Also: N00-N07 with fourth character .7; - N05.7 Unspecified nephritic syndrome with diffuse crescentic glomerulonephritis
      • endocapillary proliferative - See Also: N00-N07 with fourth character .4; - N05.4 Unspecified nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis
      • membranous - See Also: N00-N07 with fourth character .2; - N05.2 Unspecified nephritic syndrome with diffuse membranous glomerulonephritis
      • mesangial proliferative - See Also: N00-N07 with fourth character .3; - N05.3 Unspecified nephritic syndrome with diffuse mesangial proliferative glomerulonephritis
      • mesangiocapillary - See Also: N00-N07 with fourth character .5; - N05.5 Unspecified nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
      • sclerosing - N18.9 Chronic kidney disease, unspecified
    • endocapillary proliferative (diffuse) NEC - See Also: N00-N07 with fourth character .4; - N05.4 Unspecified nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis
    • extracapillary NEC - See Also: N00-N07 with fourth character .7; - N05.7 Unspecified nephritic syndrome with diffuse crescentic glomerulonephritis
    • focal (and segmental) - See Also: N00-N07 with fourth character .1; - N05.1 Unspecified nephritic syndrome with focal and segmental glomerular lesions
    • hypocomplementemic - See: Glomerulonephritis, membranoproliferative;
    • IgA - See: Nephropathy, IgA;
    • immune complex (circulating) NEC - N05.8 Unspecified nephritic syndrome with other morphologic changes
    • in (due to)
      • amyloidosis - E85.4 Organ-limited amyloidosis
      • bilharziasis - B65.9 Schistosomiasis, unspecified
      • cryoglobulinemia - D89.1 Cryoglobulinemia
      • defibrination syndrome - D65 Disseminated intravascular coagulation [defibrination syndrome]
      • diabetes mellitus - See: Diabetes, glomerulosclerosis;
      • disseminated intravascular coagulation - D65 Disseminated intravascular coagulation [defibrination syndrome]
      • Fabry (-Anderson) disease - E75.21 Fabry (-Anderson) disease
      • Goodpasture's syndrome - M31.0 Hypersensitivity angiitis
      • hemolytic-uremic syndrome - D59.3 Hemolytic-uremic syndrome
      • Henoch (-Schönlein) purpura - D69.0 Allergic purpura
      • lecithin cholesterol acyltransferase deficiency - E78.6 Lipoprotein deficiency
      • microscopic polyangiitis - M31.7 Microscopic polyangiitis
      • multiple myeloma - C90.0 Multiple myeloma
      • Plasmodium malariae - B52.0 Plasmodium malariae malaria with nephropathy
      • schistosomiasis - B65.9 Schistosomiasis, unspecified
      • sepsis - A41.9 Sepsis, unspecified organism
        • streptococcal - A40 Streptococcal sepsis
      • sickle-cell disorders - D57.
      • strongyloidiasis - B78.9 Strongyloidiasis, unspecified
      • subacute bacterial endocarditis - I33.0 Acute and subacute infective endocarditis
      • syphilis (late) congenital - A50.59 Other late congenital syphilis, symptomatic
      • systemic lupus erythematosus - M32.14 Glomerular disease in systemic lupus erythematosus
      • thrombotic thrombocytopenic purpura - M31.1 Thrombotic microangiopathy
      • typhoid fever - A01.09 Typhoid fever with other complications
      • Waldenström macroglobulinemia - C88.0 Waldenstrom macroglobulinemia
      • Wegener's granulomatosis - M31.31 Wegener's granulomatosis with renal involvement
    • latent or quiescent - N03.9 Chronic nephritic syndrome with unspecified morphologic changes
    • lobular, lobulonodular - See: Glomerulonephritis, membranoproliferative;
    • membranoproliferative (diffuse) (type 1 or 3) - See Also: N00-N07 with fourth character .5; - N05.5 Unspecified nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
      • dense deposit (type 2) NEC - See Also: N00-N07 with fourth character .6; - N05.6 Unspecified nephritic syndrome with dense deposit disease
    • membranous (diffuse) NEC - See Also: N00-N07 with fourth character .2; - N05.2 Unspecified nephritic syndrome with diffuse membranous glomerulonephritis
    • mesangial
      • IgA/IgG - See: Nephropathy, IgA;
      • proliferative (diffuse) NEC - See Also: N00-N07 with fourth character .3; - N05.3 Unspecified nephritic syndrome with diffuse mesangial proliferative glomerulonephritis
    • mesangiocapillary (diffuse) NEC - See Also: N00-N07 with fourth character .5; - N05.5 Unspecified nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
    • necrotic, necrotizing NEC - See Also: N00-N07 with fourth character .8; - N05.8 Unspecified nephritic syndrome with other morphologic changes
    • nodular - See: Glomerulonephritis, membranoproliferative;
    • poststreptococcal NEC - N05.9 Unspecified nephritic syndrome with unspecified morphologic changes
      • acute - N00.9 Acute nephritic syndrome with unspecified morphologic changes
      • chronic - N03.9 Chronic nephritic syndrome with unspecified morphologic changes
      • rapidly progressive - N01.9 Rapidly progressive nephritic syndrome with unspecified morphologic changes
    • proliferative NEC - See Also: N00-N07 with fourth character .8; - N05.8 Unspecified nephritic syndrome with other morphologic changes
      • diffuse (lupus) - M32.14 Glomerular disease in systemic lupus erythematosus
    • rapidly progressive - N01.9 Rapidly progressive nephritic syndrome with unspecified morphologic changes
    • sclerosing, diffuse - N18.9 Chronic kidney disease, unspecified
    • specified pathology NEC - See Also: N00-N07 with fourth character .8; - N05.8 Unspecified nephritic syndrome with other morphologic changes
    • subacute - N01.9 Rapidly progressive nephritic syndrome with unspecified morphologic changes
    • with
      • C3
        • glomerulonephritis - N05.A Unspecified nephritic syndrome with C3 glomerulonephritis
        • glomerulopathy - N05.A Unspecified nephritic syndrome with C3 glomerulonephritis
          • with dense deposit disease - N05.6 Unspecified nephritic syndrome with dense deposit disease
      • edema - See: Nephrosis;
      • minimal change - N05.0 Unspecified nephritic syndrome with minor glomerular abnormality
      • minor glomerular abnormality - N05.0 Unspecified nephritic syndrome with minor glomerular abnormality

Applicable Clinical Terms Definitions

Amyloidosis: A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits.

Cryoglobulinemia: A condition characterized by the presence of abnormal quantities of CRYOGLOBULINS in the blood. Upon cold exposure, these abnormal proteins precipitate into the microvasculature leading to restricted blood flow in the exposed areas.

Diabetes Mellitus: A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE.

Disseminated Intravascular Coagulation: A disorder characterized by procoagulant substances entering the general circulation causing a systemic thrombotic process. The activation of the clotting mechanism may arise from any of a number of disorders. A majority of the patients manifest skin lesions, sometimes leading to PURPURA FULMINANS.

Edema: Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE.

Glomerulonephritis: 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.

Hemolytic-Uremic Syndrome: A syndrome that is associated with microvascular diseases of the KIDNEY, such as RENAL CORTICAL NECROSIS. It is characterized by hemolytic anemia (ANEMIA, HEMOLYTIC); THROMBOCYTOPENIA; and ACUTE RENAL FAILURE.

Multiple Myeloma: A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY.

Plasmodium malariae: A protozoan parasite that occurs primarily in subtropical and temperate areas. It is the causal agent of quartan malaria. As the parasite grows it exhibits little ameboid activity.

Schistosomiasis: Infection with flukes (trematodes) of the genus SCHISTOSOMA. Three species produce the most frequent clinical diseases: SCHISTOSOMA HAEMATOBIUM (endemic in Africa and the Middle East), SCHISTOSOMA MANSONI (in Egypt, northern and southern Africa, some West Indies islands, northern 2/3 of South America), and SCHISTOSOMA JAPONICUM (in Japan, China, the Philippines, Celebes, Thailand, Laos). S. mansoni is often seen in Puerto Ricans living in the United States.

Sepsis: Systemic inflammatory response syndrome with a proven or suspected infectious etiology. When sepsis is associated with organ dysfunction distant from the site of infection, it is called severe sepsis. When sepsis is accompanied by HYPOTENSION despite adequate fluid infusion, it is called SEPTIC SHOCK.

Strongyloidiasis: Infection with nematodes of the genus STRONGYLOIDES. The presence of larvae may produce pneumonitis and the presence of adult worms in the intestine could lead to moderate to severe diarrhea.

Endocarditis, Subacute Bacterial: ENDOCARDIUM infection that is usually caused by STREPTOCOCCUS. Subacute infective endocarditis evolves over weeks and months with modest toxicity and rare metastatic infection.

Typhoid Fever: An acute systemic febrile infection caused by SALMONELLA TYPHI, a serotype of SALMONELLA ENTERICA.

Granulomatosis with Polyangiitis: A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN.