N03.9 ICD-10-CM Code: Chronic nephritic syndrome with unspecified morphologic changes
Billing Status: YES. This is a valid, specific, and billable ICD-10-CM reference.
Coding at a Glance
- Tabular directives
- 3 inclusion terms · 4 Excludes1 · 1 code-also instruction
Inpatient Payment Groups (MS-DRG)
Potential MS-DRG participation — not a DRG assignment.
MS-DRGs this diagnosis helps define, as principal or secondary, per the CMS ICD-10-CM/PCS MS-DRG Definitions Manual v43, Appendix B.
- MS-DRG 698 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH MCC (MDC 11)
- MS-DRG 699 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH CC (MDC 11)
- MS-DRG 700 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITHOUT CC/MCC (MDC 11)
A diagnosis appearing in a group's logic does not by itself determine the DRG assigned to a stay; the grouper uses the full claim.
Coding instructions
Official Tabular Instructional Notes: the inclusion, exclusion and sequencing notes published for N03.9 in the official ICD-10-CM tabular list, quoted as published.
Source: CMS/CDC — ICD-10-CM Tabular ListRelease: FY2026Effective: October 1, 2025
Notes without a marker are published on N03.9 itself; “inherited from” names the category or block whose note applies here.
Includes
Conditions the official ICD-10-CM tabular list includes under this code.
- chronic glomerular disease
- chronic glomerulonephritis
- chronic nephritis
Source: inherited from N03
Excludes1 — Not Coded Here
Conditions generally not reported together with this code (Excludes1) -- an error unless the two conditions are documented as unrelated to each other (ICD-10-CM Official Guidelines, Section I.A.12.a).
- chronic tubulo-interstitial nephritis (N11.-) inherited from N03Compare N03.9 vs N11 →
- diffuse sclerosing glomerulonephritis (N05.8-) inherited from N03Compare N03.9 vs N05.8 →
- nephritic syndrome NOS (N05.-) inherited from N03Compare N03.9 vs N05 →
- hypertensive chronic kidney disease (I12.-) inherited from N00-N08Compare N03.9 vs I12 →
Coder workflow for N03.9
MedCoder structured workflow — derived from this code’s own official record
Before you code N03.9
- Unspecified does not mean incorrect. When the record gives no greater specificity, N03.9 may be the appropriate code. Check the record for detail that supports a more specific sibling — in this subcategory the siblings differ by acute versus chronic, the presence or absence of the associated condition. An unspecified code is for records that do not provide the detail a more specific code needs; a query, not an assumption, is the route to specificity (Guidelines I.A.9.b, I.B.18).
ReviewN03.0, N03.1, N03.2, N03.3, N03.4, N03.5, N03.6, N03.7
See the relationships section · Guide: Other vs unspecified (NEC vs NOS) →
- N03.9’s title joins a condition with an associated condition or complication. Confirm each component is documented. Where the classification presumes the link through the “with” convention, only a provider statement that the conditions are unrelated defeats it. A combination code is assigned only when it fully identifies the documented conditions; a required second code for the stage, type or manifestation is still reported when the notes ask for it (Guidelines I.B.9, I.A.15).
- Check the Excludes1 note: if the documentation supports a condition named there, do not simply proceed with N03.9. Excludes1 conditions are not reported together with this code unless the record shows they are unrelated (Guidelines I.A.12.a).
Choose the right path
- Does the record document the detail a more specific sibling code needs?
Yes → Review the specific siblings in this subcategory.
No → Continue — N03.9 is appropriate when the documentation goes no further.ReviewN03.0, N03.1, N03.2, N03.3, N03.4, N03.5, N03.6, N03.7
- Does the documentation support a condition named in N03.9’s Excludes1 note?
Yes → Do not simply proceed: review the excluded code. Both are reported only when the record shows the two conditions are unrelated.
No → Continue.
Consider N03.9. Then review the Code Also note, and confirm the code is valid for the date of service in the Verify section.
Documentation check
- The provider’s diagnostic statement
- Codes are assigned from the provider’s documented diagnosis, not from clinical criteria, test values or a medication list (Guidelines I.A.19).
- Acuity
- Acute or chronic as documented; when both are documented and separate codes exist, both are reported with the acute code first (Guidelines I.B.8).
- The associated condition or complication
- Whether the associated condition the title names is documented; the “with” convention presumes some links, and a provider statement that the conditions are unrelated defeats it (Guidelines I.A.15).
- Any detail beyond this code’s title
- What the record states that a more specific sibling code would capture — or its absence, which itself supports the unspecified code.
Official instructions as workflow
Excludes1 — check before selecting N03.9(4 notes)
Coding workflow: If the documentation supports a condition named in this note, do not simply proceed with N03.9: the two are not reported together. The one exception is when the record shows the two conditions are unrelated to each other.
See the official tabular notes · Guidelines I.A.12.a
Code Also — related condition(1 note)
Coding workflow: Review the related condition when both are documented and the instruction applies. A Code Also note does not fix sequencing; the order follows the circumstances of the encounter.
See the official tabular notes · Guidelines I.A.17
Coding decision scenarios
Pattern scenarios for this code’s structure — decision rules, not clinical cases
Documentation: The provider documents the condition in the terms of this code’s title and records no further detail.
Coding question: Is a more specific sibling code supportable?
Path: Review the specific siblings in this subcategory and what each requires the record to state.
Reason: A more specific code needs documentation of the distinguishing element; without it the unspecified code is appropriate, and a provider query is the route to specificity (Guidelines I.A.9.b, I.B.18).
ReviewN03.0, N03.1, N03.2, N03.3, N03.4, N03.5, N03.6, N03.7
Documentation: Both the condition N03.9 describes and a condition named in its Excludes1 note are documented for the same encounter.
Coding question: Can both codes be reported?
Path: Review the Excludes1 note and the excluded code, and look for a provider statement on whether the two conditions are related.
Reason: Excludes1 means the two are not coded together; the exception is when the record shows the conditions are unrelated to each other (Guidelines I.A.12.a).
Documentation: Only one of the components this code’s title joins is documented.
Coding question: Is N03.9 supported?
Path: Review the code for the documented component on its own.
Reason: A combination code is assigned only when it fully identifies the documented conditions; otherwise the documented component takes its own code (Guidelines I.B.9).
Every row is derived from this code’s own record — its title, tabular notes, 7th-character family and same-category siblings — with fixed MedCoder wording; nothing is inferred about a patient. The official notes and guideline text are in the sections each row links to, and they control.
Code Overview
MedCoder summary Summary composed by MedCoder from this code's official ICD-10-CM record. The tabular instructional notes themselves appear verbatim below.
Indexed Clinical Terms (9)
Official source data — entries quoted as published, in the Index’s own lookup phrasing
Clinical term phrases from the official ICD-10-CM Index to Diseases and Injuries that map to this code. These are alphabetic-index entries shown as the Index writes them — lookup phrasing, not necessarily the wording of a final diagnosis.
- Glomerulonephritis, chronic
- Glomerulonephritis, latent or quiescent
- Glomerulonephritis, poststreptococcal NEC, chronic
- Nephritis, nephritic (albuminuric) (azotemic) (congenital) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic), atrophic
- Nephritis, nephritic (albuminuric) (azotemic) (congenital) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic), chronic
- Nephritis, nephritic (albuminuric) (azotemic) (congenital) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic), poststreptococcal, chronic
- Small (ness), white kidney
- Syndrome, nephritic, chronic
- White, kidney, small
Verify Before Coding
- CC as a secondary diagnosis (FY2026). Can raise the stay's MS-DRG severity tier.
From the code registry, the Medicare Code Editor, and the MS-DRG Definitions Manual. Check it against a full claim in Claim Check.
Relationships & Classification
MedCoder structured relationships — computed from published CMS and AHRQ datasets
MS-DRG Grouper Relationships (FY2026)
Potential MS-DRG participation — not a DRG assignment.
FY2026 MS-DRG: CC — Complication or Comorbidity. Reported as a secondary diagnosis, this code raises the stay's MS-DRG severity tier — except when the principal diagnosis is one of 277 clinically related codes on its CMS exclusion list.
Named in the grouper logic of 3 MS-DRGs: DRG 698 (MDC 11), DRG 699 (MDC 11), DRG 700 (MDC 11).
From the CMS MS-DRG Definitions Manual (Appendices B and C). Actual DRG assignment depends on the complete claim.
Clinical classification (AHRQ CCSR):GEN001 — Nephritis; nephrosis; renal sclerosis (default).
Clinical Classifications Software Refined (CCSR) for ICD-10-CM Diagnoses. Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality.
Related Codes
Same clinical process (MS-DRG)
Acts as CC — raises the severity of other admissions. CMS groups these diagnoses into one MS-DRG principal-diagnosis exclusion process — a CC/MCC on this list never raises severity when the principal diagnosis is also on it.
N02.B9 — Other recurrent and persistent immunoglobulin A nephropathy, N03.0 — Chronic nephritic syndrome with minor glomerular abnormality, N03.1 — Chronic nephritic syndrome with focal and segmental glomerular lesions, N03.2 — Chronic nephritic syndrome with diffuse membranous glomerulonephritis, N03.3 — Chronic nephritic syndrome with diffuse mesangial proliferative glomerulonephritis, N03.4 — Chronic nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis, N03.5 — Chronic nephritic syndrome with diffuse mesangiocapillary glomerulonephritis, N03.6 — Chronic nephritic syndrome with dense deposit disease, N03.7 — Chronic nephritic syndrome with diffuse crescentic glomerulonephritis, N03.8 — Chronic nephritic syndrome with other morphologic changes, N03.A — Chronic nephritic syndrome with C3 glomerulonephritis, N04.0 — Nephrotic syndrome with minor glomerular abnormality, N04.1 — Nephrotic syndrome with focal and segmental glomerular lesions, N04.20 — Nephrotic syndrome with diffuse membranous glomerulonephritis, unspecified, N04.21 — Primary membranous nephropathy with nephrotic syndrome, N04.22 — Secondary membranous nephropathy with nephrotic syndrome, N04.29 — Other nephrotic syndrome with diffuse membranous glomerulonephritis, N04.3 — Nephrotic syndrome with diffuse mesangial proliferative glomerulonephritis, N04.4 — Nephrotic syndrome with diffuse endocapillary proliferative glomerulonephritis, N04.5 — Nephrotic syndrome with diffuse mesangiocapillary glomerulonephritis, +256 more
Same clinical category (CCSR)
AHRQ's Clinical Classifications Software groups these diagnoses under the same clinical category (Nephritis; nephrosis; renal sclerosis).
N02.B9 — Other recurrent and persistent immunoglobulin A nephropathy, N03.0 — Chronic nephritic syndrome with minor glomerular abnormality, N03.1 — Chronic nephritic syndrome with focal and segmental glomerular lesions, N03.2 — Chronic nephritic syndrome with diffuse membranous glomerulonephritis, N03.3 — Chronic nephritic syndrome with diffuse mesangial proliferative glomerulonephritis, N03.4 — Chronic nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis, N03.5 — Chronic nephritic syndrome with diffuse mesangiocapillary glomerulonephritis, N03.6 — Chronic nephritic syndrome with dense deposit disease, N03.7 — Chronic nephritic syndrome with diffuse crescentic glomerulonephritis, N03.8 — Chronic nephritic syndrome with other morphologic changes, N03.A — Chronic nephritic syndrome with C3 glomerulonephritis, N04.0 — Nephrotic syndrome with minor glomerular abnormality, N04.1 — Nephrotic syndrome with focal and segmental glomerular lesions, N04.2 — Nephrotic syndrome with diffuse membranous glomerulonephritis, N04.20 — Nephrotic syndrome with diffuse membranous glomerulonephritis, unspecified, N04.21 — Primary membranous nephropathy with nephrotic syndrome, N04.22 — Secondary membranous nephropathy with nephrotic syndrome, N04.29 — Other nephrotic syndrome with diffuse membranous glomerulonephritis, N04.3 — Nephrotic syndrome with diffuse mesangial proliferative glomerulonephritis, N04.4 — Nephrotic syndrome with diffuse endocapillary proliferative glomerulonephritis, +112 more
Same Index main term, other category
The ICD-10-CM Index to Diseases and Injuries files this code under the main terms “Nephritis, nephritic”, “Glomerulonephritis”; these codes share that main term but sit in a different category of the Tabular List.
N01.1 — Rapidly progressive nephritic syndrome with focal and segmental glomerular lesions (rapidly progressive, with, focal and segmental glomerular lesions), N01.2 — Rapidly progressive nephritic syndrome with diffuse membranous glomerulonephritis (rapidly progressive, with, diffuse, membranous glomerulonephritis), N01.3 — Rapidly progressive nephritic syndrome with diffuse mesangial proliferative glomerulonephritis (rapidly progressive, with, diffuse, mesangial proliferative glomerulonephritis), N01.4 — Rapidly progressive nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis (rapidly progressive, with, diffuse, endocapillary proliferative glomerulonephritis), N01.5 — Rapidly progressive nephritic syndrome with diffuse mesangiocapillary glomerulonephritis (rapidly progressive, with, diffuse, mesangiocapillary glomerulonephritis), N01.6 — Rapidly progressive nephritic syndrome with dense deposit disease (rapidly progressive, with, dense deposit disease), N01.7 — Rapidly progressive nephritic syndrome with diffuse crescentic glomerulonephritis (rapidly progressive, with, diffuse, crescentic glomerulonephritis), N01.8 — Rapidly progressive nephritic syndrome with other morphologic changes (rapidly progressive, with, specified morphological changes NEC), N01.9 — Rapidly progressive nephritic syndrome with unspecified morphologic changes (subacute), N01.A — Rapidly progressive nephritic syndrome with C3 glomerulonephritis (rapidly progressive, with, C3, glomerulopathy), N04.9 — Nephrotic syndrome with unspecified morphologic changes (with, foot process disease), N04.B1 — Nephrotic syndrome with idiopathic immune complex membranoproliferative glomerulonephritis (IC-MPGN) (with, glomerular lesion, idiopathic immune membranoproliferative glomerulonephritis), N04.B2 — Nephrotic syndrome with secondary immune complex membranoproliferative glomerulonephritis (IC-MPGN) (with, glomerular lesion, secondary immune complex membranoproliferative glomerulonephritis), N05.0 — Unspecified nephritic syndrome with minor glomerular abnormality (minimal change), N05.1 — Unspecified nephritic syndrome with focal and segmental glomerular lesions (focal), N05.2 — Unspecified nephritic syndrome with diffuse membranous glomerulonephritis (membranous NEC), N05.3 — Unspecified nephritic syndrome with diffuse mesangial proliferative glomerulonephritis (mesangial, proliferative NEC), N05.4 — Unspecified nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis (endocapillary proliferative NEC), N05.5 — Unspecified nephritic syndrome with diffuse mesangiocapillary glomerulonephritis (mesangiocapillary NEC), N05.6 — Unspecified nephritic syndrome with dense deposit disease (dense deposit), +74 more
Lab tests where this diagnosis supports Medicare coverage (NCD)
Medicare's National Coverage Determination (NCD) program lists this diagnosis as medical justification for these lab tests.
Contextual Map
Every relationship of N03.9 in one view: hierarchy, official tabular instructions in both directions, clinical classification, risk adjustment, MS-DRG participation, index terms and change history — each edge carrying the CMS source it derives from.
Hierarchy
- N00-N99 — Chapter 14: Diseases of the Genitourinary System (N00-N99) (N00-N99)[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- N00-N08 — Glomerular diseases[Hierarchy]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
Clinical classification (CCSR)
- GEN001 — Nephritis; nephrosis; renal sclerosis[CCSR]— AHRQ CCSR for ICD-10-CM Diagnoses (HCUP)
MS-DRG Grouper
- CC — Complication or Comorbidity [MS-DRG severity]: “As a secondary diagnosis this code can raise the stay's MS-DRG severity tier (CC).”— CMS MS-DRG Definitions Manual (Appendix C) · FY2026
- DRG 698 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH MCC[MS-DRG]: “OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH MCC (MDC 11)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 699 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH CC[MS-DRG]: “OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITH CC (MDC 11)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
- DRG 700 — OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITHOUT CC/MCC[MS-DRG]: “OTHER KIDNEY AND URINARY TRACT DIAGNOSES WITHOUT CC/MCC (MDC 11)”— CMS MS-DRG Definitions Manual (Appendix B) · FY2026
MDC crossing
- MDC 11 — Diseases and Disorders of the Kidney and Urinary Tract[MDC crossing]: “Diseases and Disorders of the Kidney and Urinary Tract — the grouper's crossing between diagnoses and procedures: a principal diagnosis sets the MDC, and same-MDC procedures move the stay to its surgical DRGs. 3,574 same-MDC procedures group here; browse them on the MDC page.”— CMS MS-DRG Definitions Manual · FY2026
Index entries (9)
- Glomerulonephritis, chronic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Glomerulonephritis, latent or quiescent[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Glomerulonephritis, poststreptococcal NEC, chronic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Nephritis, nephritic (albuminuric) (azotemic) (congenital) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic), atrophic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Nephritis, nephritic (albuminuric) (azotemic) (congenital) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic), chronic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Nephritis, nephritic (albuminuric) (azotemic) (congenital) (disseminated) (epithelial) (familial) (focal) (granulomatous) (hemorrhagic) (infantile) (nonsuppurative, excretory) (uremic), poststreptococcal, chronic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Small (ness), white kidney[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- Syndrome, nephritic, chronic[Index term]— CMS ICD-10-CM Index to Diseases and Injuries · icd10cm-fy2026
- and 1 more
Nearest codes (11)
- N03 — Chronic nephritic syndrome[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- N03.0 — Chronic nephritic syndrome with minor glomerular abnormality[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- N03.1 — Chronic nephritic syndrome with focal and segmental glomerular lesions[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- N03.2 — Chronic nephritic syndrome with diffuse membranous glomerulonephritis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- N03.3 — Chronic nephritic syndrome with diffuse mesangial proliferative glomerulonephritis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- N03.4 — Chronic nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- N03.5 — Chronic nephritic syndrome with diffuse mesangiocapillary glomerulonephritis[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- N03.6 — Chronic nephritic syndrome with dense deposit disease[Sibling]— CMS ICD-10-CM tabular structure · icd10cm-fy2026
- and 3 more
Change history
- FY2016 — In the code set at ICD-10-CM adoption [Change history]— CMS release files (code change ledger) · icd10cm-fy2016
Sources for this page
Codes, titles, notes, index terms and mappings on this page are transcribed from the datasets below. Relationships MedCoder computed and text MedCoder wrote are labelled where they appear.
- Code, title, tabular notes and index terms Official source data
- CMS/CDC ICD-10-CM FY2026 tabular list, index and tables, effective October 1, 2025 Release, file and checksum · Publisher’s page
- Claim edits Official source data
- CMS Definitions of Medicare Code Edits — v43.1 (April 2026) Release, file and checksum · Publisher’s page
- Inpatient payment groups Official source data
- CMS MS-DRG Definitions Manual (incl. Appendix B diagnosis index, Appendix C CC/MCC list, Appendix E procedure index) and IPPS Final Rule tables — v43 Release, file and checksum · Publisher’s page
- Change history and date-of-service validity Official source data
- CMS ICD-10-CM release addenda, ingested release by release into the change ledger Release, file and checksum · Publisher’s page
- Comparisons, relationships and the contextual map MedCoder structured relationship
- Computed by MedCoder from the tabular notes and tables above; every derived relationship is marked as derived where it appears
- Summary and FAQ answers MedCoder explanation
- Written by MedCoder to explain the sources above: drafted with AI assistance, checked by a person against the release files, and labelled as MedCoder text where it appears. Not official text.
Labels on this page: Official source data · MedCoder structured relationship · MedCoder explanation. How to read the labels · All data sources and release dates
Cite this page
Reference this page in a research guide, syllabus or article. The release is included because code content changes each year.
MedCoder.ai. "N03.9 — Chronic nephritic syndrome with unspecified morphologic changes." ICD-10-CM FY2026. https://medcoder.ai/icd10/code/n03.9-chronic-nephritic-syndrome-with-unspecified-morphologic-changes
Change history
- FY2016 — October 1, 2015In the code set at ICD-10-CM adoptionChronic nephritic syndrome with unspecified morphologic changes
No changes since FY2016 — additions, deletions, description changes and billable-status changes are tracked through FY2027 (effective October 1, 2026), and none are recorded for this code. Note changes are tracked from FY2027 only.
Nearest Codes in This Family
Official ICD-10-CM classifications closest to N03.9 in its code family, with their registry titles.
- N03.0 — Chronic nephritic syndrome with minor glomerular abnormality
- N03.1 — Chronic nephritic syndrome with focal and segmental glomerular lesions
- N03.2 — Chronic nephritic syndrome with diffuse membranous glomerulonephritis
- N03.3 — Chronic nephritic syndrome with diffuse mesangial proliferative glomerulonephritis
- N03.4 — Chronic nephritic syndrome with diffuse endocapillary proliferative glomerulonephritis
- N03.5 — Chronic nephritic syndrome with diffuse mesangiocapillary glomerulonephritis
- N03.6 — Chronic nephritic syndrome with dense deposit disease
- N03.7 — Chronic nephritic syndrome with diffuse crescentic glomerulonephritis
- N03.8 — Chronic nephritic syndrome with other morphologic changes
- N03.A — Chronic nephritic syndrome with C3 glomerulonephritis