Autoimmune liver disease

Description

Autoimmune liver diseases are generally forms of chronic liver disease in which the etiology is unclear but autoimmune mechanisms are evident or postulated for the development of the disease. The primary target organ is the liver and/or biliary system. It can progress to liver cirrhosis.

Exclusions from above levels

ME10.1 – Unspecified jaundice
01 – Certain infectious or parasitic diseases
02 – Neoplasms

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05 – Endocrine, nutritional or metabolic diseases
06 – Mental, behavioural or neurodevelopmental disorders
18 – Complications of pregnancy, childbirth and the puerperium
22 – Injury, poisoning or certain other consequences of external causes

Child codes

DB96.0 – Autoimmune hepatitis
DB96.1 – Primary biliary cholangitis
DB96.2 – Primary sclerosing cholangitis
DB96.Y – Other specified autoimmune liver disease
DB96.Z – Autoimmune liver disease, unspecified

Sibling codes

DB90 – Infectious liver disease
DB91 – Acute or subacute hepatic failure
DB92 – Non-alcoholic fatty liver disease
DB93 – Hepatic fibrosis or cirrhosis
DB94 – Alcoholic liver disease
DB95 – Drug-induced or toxic liver disease
DB97 – Certain specified inflammatory liver diseases
DB98 – Vascular disorders of the liver
DB99 – Certain specified diseases of liver
DB9Z – Diseases of liver, unspecified

Foundation entity

Autoimmune liver disease – http://id.who.int/icd/entity/1057142191

Allowed postcoordination axes

Part of: 13: Diseases of the digestive system