2026 ICD-10-CM Diagnosis Code N07.8Hereditary nephropathy, not elsewhere classified with other morphologic lesions
ICD-10-CM Codes›N00–N99›N00-N08›N07
- Billable — Valid for Submission
- Chronic Condition
N07.8 is a billable ICD-10-CM diagnosis code for hereditary nephropathy, not elsewhere classified with other morphologic lesions. 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 fibronectin glomerulopathy. 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.
- Fibronectin glomerulopathy
- Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation
- Glomerulopathy with fibronectin deposits 1
- Thyrocerebrorenal syndrome
Tabular List NotesGuidance
Coding notes and annotation back-references applicable to this code.
Inclusion Terms
- Hereditary nephropathy, not elsewhere classified with proliferative glomerulonephritis NOS
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
- specified morphological changes NEC - N07.8
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Nephropathy
- hereditary NEC
- with
- specified morphological changes NEC
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
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 N07.8 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code History & ChangesHistory
Replaced This code was replaced in the FY 2026 code set by:
- N07.B - Hereditary nephrop, NEC with APOL1-mediated kidney disease
- N07.B - Hereditary nephrop, NEC with APOL1-mediated kidney disease
Questions About N07.8Overview
Is N07.8 (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 other morphologic lesions on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does N07.8 group to?
When hereditary nephropathy, not elsewhere classified with other morphologic lesions 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 N07.8?
Under the General Equivalence Mappings, hereditary nephropathy, not elsewhere classified with other morphologic lesions 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.
