Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis
ICD-10 N07.2 is a billable code used to indicate a diagnosis of hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis.
N07.2 refers to a specific type of hereditary nephropathy characterized by diffuse membranous glomerulonephritis, a condition where the glomeruli (the filtering units of the kidney) become inflamed and thickened due to the deposition of immune complexes. This condition can lead to isolated proteinuria, which is the presence of excess protein in the urine without significant hematuria (blood in urine) or renal impairment. The hereditary aspect indicates a genetic predisposition, often linked to mutations in genes responsible for kidney function. Patients may present with symptoms such as edema, hypertension, and varying degrees of renal dysfunction. Genetic testing may be warranted to identify specific mutations associated with the nephropathy, which can guide management and family planning. The complexity of this condition lies in its varied presentation and the need for thorough genetic evaluation to differentiate it from other glomerular disorders.
Detailed clinical notes including lab results, imaging studies, and genetic testing outcomes.
Patients presenting with proteinuria, edema, and hypertension; family history of kidney disease.
Ensure comprehensive documentation of renal function tests and any interventions performed.
Genetic testing results, family pedigree charts, and clinical correlation with nephrology findings.
Patients with a family history of hereditary nephropathy seeking genetic counseling.
Document the rationale for genetic testing and any implications for family members.
When a patient is suspected of having hereditary nephropathy based on clinical presentation.
Document the indication for testing and results.
Nephrology specialists should ensure that genetic testing is clearly linked to the diagnosis.
Genetic testing is crucial for confirming the hereditary nature of the nephropathy, identifying specific mutations, and guiding treatment options.
