2026 ICD-10-CM Diagnosis Code N07.7Hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis
ICD-10-CM Codes›N00–N99›N00-N08›N07
- Billable — Valid for Submission
- Chronic Condition
N07.7 is a billable ICD-10-CM diagnosis code for hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 698 through 700. Coders also document this condition as diffuse crescentic glomerulonephritis. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Nephritis; nephrosis; renal sclerosis.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Diffuse crescentic glomerulonephritis
- Hereditary diffuse crescentic glomerulonephritis
- Idiopathic crescentic glomerulonephritis
Tabular List NotesGuidance
Coding notes and annotation back-references applicable to this code.
Inclusion Terms
- Hereditary nephropathy, not elsewhere classified with extracapillary glomerulonephritis
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Nephropathy - See Also: Nephritis; - N28.9
- hereditary NEC - N07.9
- with
- diffuse
- crescentic glomerulonephritis - N07.7
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Nephropathy
- hereditary NEC
- with
- diffuse
- crescentic glomerulonephritis
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Idiopathic Crescentic Glomerulonephritis
crescentic glomerulonephritis, the cause of which is unknown.
Patient EducationClinical
Genetic Disorders
Genetic disorders are health conditions caused by changes (also called mutations or variants) in your genes. Genes are parts of DNA found in your cells that carry instructions for how your body grows, develops, and functions. Many genes tell your body how to make proteins, which are needed for your body to work properly.
The full article covers:
- What are genetic disorders?
- What causes genetic disorders?
- What are the types of genetic disorders?
- What are the different ways a genetic disorder can be inherited?
- How are genetic disorders diagnosed?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert N07.7 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About N07.7Overview
Is N07.7 (Hereditary nephropathy, not elsewhere classified) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does N07.7 group to?
When hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis is the principal diagnosis on an inpatient stay, it groups to MS-DRG 698, 699, 700, with relative weights from 0.6899 to 1.6544 depending on complications. Higher weights mean higher Medicare reimbursement.
What is the ICD-9 equivalent of N07.7?
Under the General Equivalence Mappings, hereditary nephropathy, not elsewhere classified with diffuse crescentic glomerulonephritis converts to ICD-9-CM 583.89 (nephritis NEC). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
