Gilbert disease Crigler-Najjar Hereditary fructose intolerance Tyrosinaemia type I Adenosylhomocysteine hydrolase Maple syrup urine disease Methylmalonic acidemia Proprionic acidemia Isovaleric acidemia Holocarboxylase synthase deficiency NAGS deficiency Carbamoylphosphate synthase deficiency OTC deficiency Arginosuccinic aciduria VLCAD deficiency LCHAD deficiency MCAD deficiency Mitochondrial disorders Zellweger syndrome Neonatal adrenoleukodystrophy Tangier disease Smith-Lemli-Opitz syndrome Mevalonate kinase deficiency GM1 gangliosidosis GM2 gangliosidosis AMSD A/B Niemann-Pick C Viral hepatitis Infectious Mononucleosis TORCH infections Parvovirus B19 Haemophagocytic lymphohistiocytosis Drug induced hepatitis Alagille syndrome Beckwith-Wiedemann syndrome McCune-Albright syndrome Septo-optic dysplasia Smith-Lemli-Optiz syndrome Langerhans cell histiocytosis Congestive cardiac failure Budd-Chiari syndrome Autoimmune liver disease Extrahepatic obstruction Primary biliary cirrhosis Primary sclerosing cholangitis Metastatic carcinoma Sickle cell disease Haemolytic anaemia Wilson's disease Glycogen storage diseases PEPCKD Citrullinaemia Abetalipoproteinaemia Gaucher Farber HIV Malaria Paracetamol Obesity Hypothyroidism Lymphoma Amyloidosis Sarcoidosis Thalassaemia Myeloma Leukaemia Haemochromatosis Galactosaemia Hepatoblastoma