N07.A — Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis
Is N07.A billable?
Yes, but N07.A is an unspecified code. N07.A is a valid, billable ICD-10-CM code for encounters from October 1, 2026 through September 30, 2027. However, N07.A is an unspecified or catch-all code. Payers apply additional scrutiny to unspecified codes and many deny them when the medical record supports a more specific option, so check the documentation before selecting N07.A — the more specific alternatives are listed below.
More specific alternatives
- N07.0Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality
- N07.1Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
- N07.2Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis
- N07.3Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
- N07.4Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
- N07.5Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
- N07.6Hereditary nephropathy, not elsewhere classified with dense deposit disease
- N07.7Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis
- N07.8Hereditary nephropathy, not elsewhere classified with other morphologic lesions
- N07.9Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions
- N07.BHereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]
N07.A at a glance
| Code | N07.A |
|---|---|
| Description | Hereditary nephropathy, not elsewhere classified with C3 glomerulonephritis |
| Billable | Yes |
| Code set | ICD-10-CM FY2027 |
| Valid for encounters | October 1, 2026 – September 30, 2027 |
Which MS-DRGs does N07.A group to?
N07.A sits in MDC 11 and helps define the logic of 3 MS-DRGs (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.
- 698Other Kidney and Urinary Tract Diagnoses with MCCmedical
- 699Other Kidney and Urinary Tract Diagnoses with CCmedical
- 700Other Kidney and Urinary Tract Diagnoses without CC/MCCmedical
As a secondary diagnosis, N07.A is a complication or comorbidity (CC), which can move a stay into a higher-paying DRG.
How is N07.A listed in the Alphabetic Index?
These are the routes through the Alphabetic Index that lead to N07.A. They show the wording a clinician may have documented, which often differs from the Tabular description.
- Nephropathy › hereditary NEC › with › C3 › glomerulonephritis
- Nephropathy › hereditary NEC › with › C3 › glomerulopathy
Excludes1 — never code together
The conditions below can never be reported together with N07.A on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
Inclusion terms
Alternative wording in documentation that is classified to N07.A.
- Hereditary nephropathy, not elsewhere classified with C3 glomerulopathy
Excludes1 — never code together — inherited from N00-N08
The conditions below can never be reported together with N07.A on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.
- hypertensive chronic kidney disease (I12.-)
Excludes2 — not included here — inherited from Chapter 14
The conditions below are not part of N07.A, but a patient may have both at the same time. When documentation supports it, N07.A and the excluded code may both be reported.
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Excludes2 — not included here — inherited from N07
The conditions below are not part of N07.A, but a patient may have both at the same time. When documentation supports it, N07.A and the excluded code may both be reported.
Code also — inherited from N00-N08
Two codes may be needed to describe the condition fully. Whether N07.A is sequenced first depends on the reason for the encounter.
- any associated kidney failure (N17-N19).
How long has N07.A existed?
N07.A first appears in FY2021 (FY2020 is not available, so it may have appeared then).
Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.
Which codes are confused with N07.A?
ICD-10-CM declares these codes mutually exclusive with N07.A — exactly one of each pair can be correct for a given encounter.
Which conditions are coded to N07.A?
What other codes are in the N07 family? (11)
- N07.0Hereditary nephropathy, not elsewhere classified with minor glomerular abnormality
- N07.1Hereditary nephropathy, not elsewhere classified with focal and segmental glomerular lesions
- N07.2Hereditary nephropathy, not elsewhere classified with diffuse membranous glomerulonephritis
- N07.3Hereditary nephropathy, not elsewhere classified with diffuse mesangial proliferative glomerulonephritis
- N07.4Hereditary nephropathy, not elsewhere classified with diffuse endocapillary proliferative glomerulonephritis
- N07.5Hereditary nephropathy, not elsewhere classified with diffuse mesangiocapillary glomerulonephritis
- N07.6Hereditary nephropathy, not elsewhere classified with dense deposit disease
- N07.7Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis
- N07.8Hereditary nephropathy, not elsewhere classified with other morphologic lesions
- N07.9Hereditary nephropathy, not elsewhere classified with unspecified morphologic lesions
- N07.BHereditary nephropathy, not elsewhere classified with APOL1-mediated kidney disease [AMKD]