Hereditary nephropathy, not elsewhere classified with dense deposit disease
ICD-10 N07.6 is a billable code used to indicate a diagnosis of hereditary nephropathy, not elsewhere classified with dense deposit disease.
N07.6 refers to hereditary nephropathy characterized by dense deposit disease, a specific type of glomerular disorder. This condition is often associated with isolated proteinuria, which is the presence of excess protein in the urine without significant hematuria or other renal symptoms. Dense deposit disease is a rare form of membranoproliferative glomerulonephritis, primarily caused by genetic mutations affecting the complement system, leading to abnormal deposition of complement components in the glomeruli. Patients may present with varying degrees of renal impairment, and the condition can progress to end-stage renal disease. Genetic testing is crucial for diagnosis and management, as it can identify specific mutations linked to hereditary nephropathy. Clinicians must differentiate this condition from other glomerular disorders classified elsewhere, ensuring accurate coding and treatment planning.
Detailed clinical notes on renal function, proteinuria levels, and genetic testing results.
Patients presenting with isolated proteinuria and family history of kidney disease.
Ensure comprehensive documentation of all renal assessments and laboratory results.
Records of genetic testing and family history of hereditary nephropathy.
Patients undergoing evaluation for hereditary kidney disorders.
Documentation must include the rationale for genetic testing and results interpretation.
Used when hereditary nephropathy is suspected based on family history.
Documentation of clinical indications for genetic testing and results.
Nephrology specialists should ensure that genetic testing is clearly linked to the diagnosis.
Genetic testing is crucial for confirming the diagnosis of hereditary nephropathy with dense deposit disease, as it identifies specific mutations that can guide treatment and management strategies.