N07.5 vs N07.A
N07.5 (Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis) compared with N07.A (Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis), from the official CMS tabular data. Do not report these codes together: the official tabular list marks them Excludes1.
Can these codes be reported together?
No — do not report together. N07.5 carries an Excludes1 note covering N07.A: “Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis (N07.A)”
Sole exception: when the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
No — do not report together. N07.5 carries an Excludes1 note covering N07.A: “Hereditary nephropathy, not elsewhere classified with C3 glomerulopathy (N07.A)”
Sole exception: when the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
Side by side
| N07.5Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis | N07.AHereditary nephropathy, not elsewhere classified with C3 glomerulonephritis | |
|---|---|---|
| Billing status | Billable | Billable |
| Classification | N00-N99 — Diseases of the Genitourinary System (N00-N99) | N00-N99 — Diseases of the Genitourinary System (N00-N99) |
| Definition | Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis is a billable ICD-10-CM diagnosis code (N07.5). | Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis is a billable ICD-10-CM diagnosis code (N07.A). |
| Includes | Hereditary nephropathy, not elsewhere classified with membranoproliferative glomerulonephritis, types 1 and 3, or NOS | Hereditary nephropathy, not elsewhere classified with C3 glomerulopathy |
Derived from the official CMS ICD-10-CM tabular data (FY2026). Not billing advice; verify sequencing rules for the encounter. All data sources