Other diseases of liver (K76)
Clinical Information
Dyspnea - Difficult or labored breathing.
Hepatic Encephalopathy - A syndrome characterized by central nervous system dysfunction in association with LIVER FAILURE, including portal-systemic shunts. Clinical features include lethargy and CONFUSION (frequently progressing to COMA); ASTERIXIS; NYSTAGMUS, PATHOLOGIC; brisk oculovestibular reflexes; decorticate and decerebrate posturing; MUSCLE SPASTICITY; and bilateral extensor plantar reflexes (see REFLEX, BABINSKI). ELECTROENCEPHALOGRAPHY may demonstrate triphasic waves. (From Adams et al., Principles of Neurology, 6th ed, pp1117-20; Plum & Posner, Diagnosis of Stupor and Coma, 3rd ed, p222-5)
Hepatic Infarction - Formation of infarct resulting from obstruction of HEPATIC ARTERY and/or PORTAL VEIN most often after LIVER TRANSPLANTATION or hepatobiliary surgery.
Hepatopulmonary Syndrome - A syndrome characterized by the clinical triad of advanced chronic liver disease, pulmonary vascular dilatations, and reduced arterial oxygenation (HYPOXEMIA) in the absence of intrinsic cardiopulmonary disease. This syndrome is common in the patients with LIVER CIRRHOSIS or portal hypertension (HYPERTENSION, PORTAL).
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.
Idiopathic Pulmonary Fibrosis - A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change.
Liver Regeneration - Repair or renewal of hepatic tissue.
Peliosis Hepatis - A vascular disease of the LIVER characterized by the occurrence of multiple blood-filled CYSTS or cavities. The cysts are lined with ENDOTHELIAL CELLS; the cavities lined with hepatic parenchymal cells (HEPATOCYTES). Peliosis hepatis has been associated with use of anabolic steroids (ANABOLIC AGENTS) and certain drugs.
Instructional Notations
Type 2 Excludes
A type 2 excludes note represents "Not included here". An excludes2 note indicates that the condition excluded is not part of the condition represented by the code, but a patient may have both conditions at the same time. When an Excludes2 note appears under a code, it is acceptable to use both the code and the excluded code together, when appropriate.
- alcoholic liver disease K70
- amyloid degeneration of liver E85
- cystic disease of liver congenital Q44.6
- hepatic vein thrombosis I82.0
- hepatomegaly NOS R16.0
- pigmentary cirrhosis of liver E83.110
- portal vein thrombosis I81
- toxic liver disease K71
Diseases of the digestive system (K00–K95)
Diseases of liver (K70-K77)
K76 Other diseases of liver
- K76.0 Fatty (change of) liver, not elsewhere classified
- K76.1 Chronic passive congestion of liver
- K76.2 Central hemorrhagic necrosis of liver
- K76.3 Infarction of liver
- K76.4 Peliosis hepatis
- K76.5 Hepatic veno-occlusive disease
- K76.6 Portal hypertension
- K76.7 Hepatorenal syndrome
K76.8 Other specified diseases of liver
- K76.81 Hepatopulmonary syndrome
- K76.82 Hepatic encephalopathy
- K76.89 Other specified diseases of liver
- K76.9 Liver disease, unspecified
Other diseases of liver (K76)