Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
ICD-10 N07.4 is a billable code used to indicate a diagnosis of hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis.
N07.4 refers to a specific type of hereditary nephropathy characterized by diffuse endocapillary proliferative glomerulonephritis. This condition is often associated with genetic mutations that affect kidney function, leading to proteinuria and potential progression to chronic kidney disease. Patients may present with isolated proteinuria, which is a key indicator of glomerular dysfunction. The hereditary nature of this nephropathy suggests a genetic predisposition, often requiring genetic testing for accurate diagnosis and management. The diffuse endocapillary proliferative pattern indicates an inflammatory response within the glomeruli, which can be identified through renal biopsy. This condition is not classified under other specific nephropathies, making accurate coding essential for proper treatment and management.
Detailed renal function tests, biopsy results, and genetic testing outcomes.
Patients presenting with unexplained proteinuria, family history of kidney disease, or abnormal renal function tests.
Ensure that genetic testing results are included in the documentation to support the hereditary diagnosis.
Genetic test results, family history documentation, and clinical findings related to hereditary nephropathy.
Patients with a known family history of kidney disease undergoing genetic evaluation.
Documentation should clearly link genetic findings to clinical symptoms and nephropathy diagnosis.
Used when a renal biopsy is performed to confirm the diagnosis of nephropathy.
Pathology report must be included in the medical record.
Nephrologists should ensure that biopsy findings correlate with clinical symptoms.
Genetic testing is crucial for confirming the hereditary nature of the nephropathy and guiding treatment options. It helps in understanding the prognosis and potential familial implications.
