A rare genetic hepatic disease characterized by massive hepatomegaly, moderate to severe transient hypertriglyceridemia and hepatic steatosis (followed by fibrosis) manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fa
hypertriglycéridémie transitoire et stéatose hépatique du nourrisson
SNOMEDCT-CA (followed by fibrosis) manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fa / 773649005
SNOMEDCT-CA (trouble) / 773649005