N07.5 Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritisBillable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.
Defines the logic of DRG(s) 698-700 in MDC 11.
583.2 Nephritis and nephropathy, not specified as acute or chronic, with lesion of membranoproliferative glomerulonephritis (approximate)N07.0 Hereditary nephropathy, not elsewhere classified with minor glomerular abnormalityN07.1 Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesionsN07.2 Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritisN07.3 Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritisN07.4 Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritisN07.5 Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis (this code)N07.6 Hereditary nephropathy, not elsewhere classified with dense deposit diseaseN07.7 Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritisN07.8 Hereditary nephropathy, not elsewhere classified with other morphologic lesionsN07.9 Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesionsN07.A Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis