DOID:0111366

• Ontology
• Class
  • owl:Thing
    • host health status
      • disease
        • additional diseases by category
          • disease of anatomical entity
            • gastrointestinal system disease
              • gastrointestinal system benign neoplasm
                • hepatobiliary benign neoplasm
                  • liver benign neoplasm
                    • hepatocellular adenoma
                      • familial hepatic adenoma
              • hepatobiliary disease
                • liver disease
                  • liver benign neoplasm
                    • hepatocellular adenoma
                      • familial hepatic adenoma
          • genetic disease
            • monogenic disease
              • autosomal genetic disease
                • autosomal recessive disease
                  • familial hepatic adenoma
        • neoplasm
          • benign neoplasm
            • cell type benign neoplasm
              • adenoma
                • hepatocellular adenoma
                  • familial hepatic adenoma
            • organ system benign neoplasm
              • endocrine organ benign neoplasm
                • liver benign neoplasm
                  • hepatocellular adenoma
                    • familial hepatic adenoma
              • gastrointestinal system benign neoplasm
                • hepatobiliary benign neoplasm
                  • liver benign neoplasm
                    • hepatocellular adenoma
                      • familial hepatic adenoma
• Annotation Property
• Data Property
• Object Property
• Individual
• Datatype

• label
  • familial hepatic adenoma ^xsd:string
• definition
  • A hepatocellular adenoma characterized by highly vascularized liver adenomas that has_material_basis_in homozygous or compound heterozygous mutation in the HNF1A gene on chromosome 12q24.31. ^xsd:string
    • dce:type
      • obo:ECO_0007645
    • oio:hasDbXref
      • url:https://www.ncbi.nlm.nih.gov/pubmed/207987 ^xsd:string
• has exact synonym
  • familial liver cell adenomas ^@en
• has_obo_namespace
  • disease_ontology ^xsd:string
• id
  • DOID:0111366 ^xsd:string
• oio:hasDbXref
  • OMIM:142330 ^xsd:string
• rdf:type
  • owl:Class
• rdfs:subClassOf
  • hepatocellular adenoma
  • autosomal recessive disease