Disease_Mapped_To_Gene Cellosaurus Disease Terminology ATP7B Gene Childhood Cancer Predisposition Study Terminology CCPS Disease Terminology Rare Non-Neoplastic Disorder Hepatolenticular Degeneration CCPS Wilson Disease Hepatolenticular Degeneration Disease or Syndrome Hepatolenticular Degeneration Wilson's Disease A rare autosomal recessive inherited disorder caused by mutations in the ATP7B gene. It is characterized by copper accumulation in the tissues, particularly brain and liver. It results in liver failure, neurologic, and psychotic manifestations. C0019202 C84756 Cellosaurus