LB20.00

ICD-11 MMS 2026-01

Fibropolycystic liver disease

Index terms

  • Fibropolycystic liver disease
  • Congenital cystic disease of liver
  • Fibrocystic disease of liver
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  • congenital cystic liver disease
  • congenital fibrocystic liver disorder
  • congenital hepatic cyst
  • fibrocystic liver disease
  • Caroli disease
  • Cystic dilatation of intrahepatic bile ducts
  • Congenital hepatic fibrosis
  • Biliary hamartoma

Excludes

  • DB99.10 – Polycystic liver disease

Exclusions from above levels

  • DB92 – Non-alcoholic fatty liver disease
  • http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Foundation children elsewhere

Sibling codes

  • LB20.0Y – Other specified structural developmental anomalies of liver
  • LB20.0Z – Structural developmental anomalies of liver, unspecified

Foundation entity

Fibropolycystic liver disease – http://id.who.int/icd/entity/557775192

Part of: LB20.0: Structural developmental anomalies of liver › LB20: Structural developmental anomalies of gallbladder, bile ducts or liver › 20: Developmental anomalies