The human ATP7B gene page (Fig. 2c), accessible from the ontology report page by clicking the gene symbol, shows annotations to Wilson disease (Fig. 2d) as well as related diseases such as acute liver failure and liver cirrhosis and phenotypes such as atypical or prolonged hepatitis, high nonceruloplasmin-bound serum copper, polyneuropathy, hepatomegaly, and hepatic failure (Fig. 2e). The gene discussed is ATP7B; the disease is Wilson disease.