Glomerular disorders in diseases classified elsewhere 1 N08 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 The 2019 edition of ICD-10-CM N08 became effective on October 1, 2018. 3 This is the American ICD-10-CM version of N08 - other international versions of ICD-10 N08 may differ.
Thin basement membrane dis Thin basement membrane disease ICD-10-CM N02.2 is grouped within Diagnostic Related Group (s) (MS-DRG v38.0): 698 Other kidney and urinary tract diagnoses with mcc
Short description: Recurrent and perst hematur w diffuse membranous glomrlneph The 2022 edition of ICD-10-CM N02.2 became effective on October 1, 2021. This is the American ICD-10-CM version of N02.2 - other international versions of ICD-10 N02.2 may differ.
N02.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Short description: Recurrent and perst hematur w diffuse membranous glomrlneph
Causes. Anti-GBM disease is an autoimmune disorder. It occurs when the immune system mistakenly attacks and destroys healthy body tissue. People with this syndrome develop substances that attack a protein called collagen in the tiny air sacs in the lungs and the filtering units (glomeruli) of the kidneys.
ICD-10-CM Code for Nephrotic syndrome with diffuse membranous glomerulonephritis N04. 2.
The ICD-10 code range for Urolithiasis N20-N23 is medical classification list by the World Health Organization (WHO).
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.
Primary membranous nephropathy (PMN) is a kidney-specific, autoimmune glomerular disease that presents with increased protein in the urine associated with a pathognomonic pattern of injury in glomeruli (Figures 1–3). Both clinical and pathogenetic aspects of the disease have been recently reviewed elsewhere (1–8).
Primary membranous nephropathy is the most common cause of nephrotic syndrome in white persons without diabetes, but it is a rare disease as defined by the European Commission on Rare Diseases (1 case per 2000 of population) or the Rare Diseases Clinical Research Network (200,000 prevalent cases in the United States).
Calculus of ureter1: Calculus of ureter.
0: Calculus of kidney.
ICD-10 code: K57. 92 Diverticulitis of intestine, part unspecified, without perforation, abscess or bleeding.
Glomerulonephritis is inflammation and damage to the filtering part of the kidneys (glomerulus). It can come on quickly or over a longer period of time. Toxins, metabolic wastes and excess fluid are not properly filtered into the urine. Instead, they build up in the body causing swelling and fatigue.
GLOMERULAR DISEASE OVERVIEW. Glomerular disease reduces the kidneys' ability to maintain a balance of certain substances in bloodstream. Normally, the kidneys filter toxins out of the bloodstream and excrete them in the urine but keep red blood cells and protein in the bloodstream.
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).
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.
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.
A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
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The incidence of the disease is estimated to be approximately 0.6-1.8 cases per million per year in both Asian and European Caucasian (more frequently affected) populations. Men and women seem equally affected.
Anti-GBM disease onset is bimodal, occurring mainly in the third and the seventh decades of life. The majority of patients (80-90%) will present with features of rapidly progressive glomerulonephritis. 40 to 60% will have concurrent lung hemorrhage, and a small minority of patients may present with isolated pulmonary disease.
Anti-GBM disease is considered to be a vasculitis affecting glomerular capillaries, pulmonary capillaries, or both, with deposition of anti-basement membrane antibodies against the non-collagenous domain 1 of the alpha 3 chain of type IV collagen (alpha3 (IV)NC1).
Diagnosis is based on the detection of anti-GBM antibodies either in serum or deposited in tissue, along with pathologic features of crescentic GN, with or without evidence of alveolar hemorrhage.
Differential diagnosis includes systemic vasculitis (e.g. Wegener's granulomatosis (GPA), microscopic polyarteritis (MPA), systemic lupus erythematosus, Churg-Strauss syndrome (EGPA)) and other vasculitides (e.g. Behçets disease, cryoglobulinemia).
Standard therapy consists in plasma exchange combined with high doses of glucocorticoids and cyclophosphamide. Recently, several reports of rituximab use have been reported, either as an adjuvant to standard therapy or as a substitute for cyclophosphamide.
Specialty: Rheumatology. MeSH Code: D019867. ICD 9 Code: 446.21.
The ICD code M310 is used to code Goodpasture syndrome. Goodpasture syndrome (GPS; also known as Goodpasture’s disease, antiglomerular basement antibody disease, or anti-GBM disease) is a rare autoimmune disease in which antibodies attack the basement membrane in lungs and kidneys, leading to bleeding from the lungs and kidney failure.