2026 ICD-10-CM Diagnosis Code K76.7Hepatorenal syndrome
ICD-10-CM Codes›K00–K95›K70-K77›K76
- Billable — Valid for Submission
- Chronic Condition
K76.7 is a billable ICD-10-CM diagnosis code for hepatorenal syndrome. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 441 through 443. Coders also document this condition as acute hepatic failure. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Acute and unspecified renal failure and Other specified and unspecified liver disease.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Acute hepatic failure
- Cholemic nephrosis
- Familial arthrogryposis-cholestatic hepatorenal syndrome
- Hepatorenal syndrome
- Hepatorenal syndrome with acute kidney injury
- Inherited disorder of bilirubin metabolism
Tabular List NotesGuidance
Coding notes and annotation back-references applicable to this code.
Type 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- hepatorenal - K76.7
- hepatorenal - K76.7
- Syndrome - See Also: Disease;
- hepatorenal - K76.7
- hepatourologic - K76.7
- Heyd's - K76.7
- liver-kidney - K76.7
- urohepatic - K76.7
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Degeneration, degenerative
- hepatorenal
- Failure, failed
- hepatorenal
- Nephrosis, nephrotic(Epstein's) (syndrome) (congenital)
- cholemic
- Syndrome
- hepatorenal
- Syndrome
- hepatourologic
- Syndrome
- Heyd's
- Syndrome
- liver-kidney
- Syndrome
- urohepatic
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Hepatorenal Syndrome
functional kidney failure in patients with liver disease, usually liver cirrhosis or portal hypertension (hypertension, portal), and in the absence of intrinsic renal disease or kidney abnormality. it is characterized by intense renal vasculature constriction, reduced renal blood flow, oliguria, and sodium retention.
Patient EducationClinical
Kidney Failure
Healthy kidneys clean your blood by removing excess fluid, minerals, and wastes. They also make hormones that keep your bones strong and your blood healthy. But if the kidneys are damaged, they don't work properly. Harmful wastes can build up in your body. Your blood pressure may rise.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert K76.7 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About K76.7Overview
Is K76.7 (Other diseases of liver) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report hepatorenal syndrome on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does K76.7 group to?
When hepatorenal syndrome is the principal diagnosis on an inpatient stay, it groups to MS-DRG 441, 442, 443, with relative weights from 0.6997 to 1.7947 depending on complications. Higher weights mean higher Medicare reimbursement.
What is the ICD-9 equivalent of K76.7?
Under the General Equivalence Mappings, hepatorenal syndrome converts to ICD-9-CM 572.4 (hepatorenal syndrome). The mapping is a direct match.
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.
