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(N07.4) Hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis
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20 599 in individuals diagnosis hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis confirmed
4 505 deaths with diagnosis hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis
22% mortality rate associated with the disease hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis
Diagnosis hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis is diagnosed Men are 13.15% more likely than Women
11 654
Men receive the diagnosis hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis
1 868 (16.0 %)Died from this diagnosis.
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Women receive the diagnosis hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis
2 637 (29.5 %)Died from this diagnosis.
Risk Group for the Disease hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis - Men and Women aged 15-19
In Men diagnosis is most often set at age 0-69, 80-84
Less common in men the disease occurs at Age 70-79, 85-95+Less common in women the disease occurs at Age 0-1, 30-39, 45-54, 80-84, 90-95+
In Women diagnosis is most often set at age 0-29, 40-44, 55-79, 85-89
Disease Features hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis
Absence or low individual and public risk
Hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis - what does this mean
Hereditary nephropathy, not elsewhere classified: diffuse endocapillary proliferative glomerulonephritis is a type of kidney disease caused by an inherited genetic mutation. this mutation leads to the inflammation and scarring of the glomeruli, which are the tiny filters in the kidneys that are responsible for filtering waste from the blood. this can lead to a decrease in kidney function, proteinuria, and eventually, kidney failure.
What happens during the disease - hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis
Hereditary nephropathy, not elsewhere classified, is a type of diffuse endocapillary proliferative glomerulonephritis that is caused by an inherited genetic mutation. this mutation affects the structure and function of the kidney, leading to an increased number of cells in the glomeruli and resulting in inflammation and scarring of the kidneys. this leads to a wide range of symptoms, including proteinuria, hematuria, hypertension, and renal failure.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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11 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis - Prevention
Prevention of hereditary nephropathy, not elsewhere classified : diffuse endocapillary proliferative glomerulonephritis involves genetic counseling, genetic testing, lifestyle modifications, and early diagnosis and treatment of any underlying conditions. it is important to reduce risk factors such as smoking, alcohol consumption, and high blood pressure. additionally, regular screenings and monitoring of kidney function is recommended.