The ICD code K74 is used to code Cirrhosis. Cirrhosis is a condition in which the liver does not function properly due to long-term damage. Typically, the disease comes on slowly over months or years. Early on, there are often no symptoms.
The ICD-10-CM is a catalog of diagnosis codes used by medical professionals for medical coding and reporting in health care settings. The Centers for Medicare and Medicaid Services (CMS) maintain the catalog in the U.S. releasing yearly updates.
ICD-10 code K74. 60 for Unspecified cirrhosis of liver is a medical classification as listed by WHO under the range - Diseases of the digestive system .
ICD-10 Code for Alcoholic cirrhosis of liver without ascites- K70. 30- Codify by AAPC.
ICD-10 code E83. 110 for Hereditary hemochromatosis is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .
31 Alcoholic cirrhosis of liver with ascites.
Alcoholic liver disease, unspecified K70. 9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM K70. 9 became effective on October 1, 2021.
ICD-10-CM Code for Liver disease, unspecified K76. 9.
572.2 - Hepatic encephalopathy. ICD-10-CM.
ICD-10 code K76. 0 for Fatty (change of) liver, not elsewhere classified is a medical classification as listed by WHO under the range - Diseases of the digestive system .
ICD-10-CM Code for Elevation of levels of liver transaminase levels R74. 01.
Cirrhosis slows the normal flow of blood through the liver, thus increasing pressure in the vein that brings blood to the liver from the intestines and spleen. Swelling in the legs and abdomen. The increased pressure in the portal vein can cause fluid to accumulate in the legs (edema) and in the abdomen (ascites).
ICD-10-CM Code for Alcoholic cirrhosis of liver with ascites K70. 31.
ICD-10 code R18. 8 for Other ascites is a medical classification as listed by WHO under the range - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified .
Idiopathic or genetic hemochromatosis is an autosomal recessive disorder of metabolism associated with a gene tightly linked to the a locus of the hla complex on chromosome 6. (from Dorland, 27th ed) An inherited metabolic disorder characterized by iron accumulation in the tissues.
A disorder due to the deposition of hemosiderin in the parenchymal cells, causing tissue damage and dysfunction of the liver, pancreas, heart, and pituitary. Full development of the disease in women is restricted by menstruation, pregnancy, and lower dietary intake of iron.