Wilson's disease (10), mitochondrial disorders (9), urea cycle disorders (4), infantile liver failures syndrome tpye 2 (NBAS) (3), tyrosinaemia type I (2), Wolcott‐Rallison syndrome (2), adenosine kinase deficiency (2), infantile liver failures syndrome tpye 1 (LARS1) (1), Progressive familial intrahepatic cholestasis (ABCB11) (1). This evidence concerns the gene ABCB11 and progressive familial intrahepatic cholestasis.