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(N07.9) Hereditary nephropathy, not elsewhere classified : unspecified
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20 599 in individuals diagnosis hereditary nephropathy, not elsewhere classified : unspecified confirmed
4 505 deaths with diagnosis hereditary nephropathy, not elsewhere classified : unspecified
22% mortality rate associated with the disease hereditary nephropathy, not elsewhere classified : unspecified
Diagnosis hereditary nephropathy, not elsewhere classified : unspecified is diagnosed Men are 13.15% more likely than Women
11 654
Men receive the diagnosis hereditary nephropathy, not elsewhere classified : unspecified
1 868 (16.0 %)Died from this diagnosis.
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8 945
Women receive the diagnosis hereditary nephropathy, not elsewhere classified : unspecified
2 637 (29.5 %)Died from this diagnosis.
Risk Group for the Disease hereditary nephropathy, not elsewhere classified : unspecified - 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 : unspecified
Absence or low individual and public risk
Hereditary nephropathy, not elsewhere classified : unspecified - what does this mean
Hereditary nephropathy, not elsewhere classified: unspecified is a type of kidney disease that is passed down from generation to generation. it is caused by a genetic mutation that affects the structure or function of the kidneys, leading to kidney damage and possible kidney failure.
What happens during the disease - hereditary nephropathy, not elsewhere classified : unspecified
Hereditary nephropathy, not elsewhere classified: unspecified is a genetic disorder that is caused by a mutation in a gene that is responsible for the development and function of the kidneys. this mutation leads to the abnormal development and function of the kidneys, causing them to be unable to filter waste products from the blood and excrete them in the urine. as a result, these waste products can accumulate in the body, leading to a range of symptoms such as high blood pressure, swelling, and proteinuria.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Complete physical examination
- Urine tests
- Blood tests
- Imaging tests (such as X-rays, CT scans, and ultrasounds)
- Kidney biopsy
- Genetic testing
Treatment and Medical Assistance
Main goal of treatment: To reduce the risk of kidney failure and slow the progression of nephropathy.
- Regular monitoring of kidney function
- Treatment of high blood pressure
- Reduction of salt and protein intake
- Regular exercise
- Weight management
- Avoiding smoking and alcohol consumption
- Use of medications to reduce proteinuria
- Regular monitoring of urine protein levels
- Monitoring for signs and symptoms of kidney failure
11 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Hereditary nephropathy, not elsewhere classified : unspecified - Prevention
Hereditary nephropathy, not elsewhere classified, unspecified can be prevented by avoiding activities that put a strain on the kidneys, such as excessive alcohol consumption, smoking, and taking certain medications. it is also important to maintain a healthy diet that is low in sodium and to maintain a healthy weight. regular exercise and avoiding exposure to environmental toxins can also help to reduce the risk of developing hereditary nephropathy.