has material basis in germline mutation in FGG familial hypofibrinogenemia inherited blood coagulation disorder hepatic fibrinogen storage disease https://github.com/monarch-initiative/mondo/issues/10238 An autosomal dominant disorder characterized by hypofibrinogenemia and variable liver disease (ranging from asymptomatic transaminase elevation to cirrhosis), caused by variants in FGG that lead to retention of variant fibrinogen as eosinophilic inclusions within the hepatocellular endoplasmic reticulum. hepatocellular fibrinogen storage disease hereditary hypofibrinogenemia with hepatic storage HHHS MONDO:7770747 HFSD