SE-ATLAS

Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Acute infantile liver failure-multisystemic involvement syndrome Alagille syndrome Alpha-1-antitrypsin deficiency Aplasia cutis congenita-intestinal lymphangiectasia syndrome Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome Autoimmune enteropathy type 2 Autoimmune enteropathy type 3 Autoimmune hepatitis Autoimmune pancreatitis Autosomal dominant polycystic kidney disease Autosomal recessive polycystic kidney disease Biliary atresia with splenic malformation syndrome Budd-Chiari syndrome CADDS Caroli disease Chronic diarrhea due to glucoamylase deficiency Chronic diarrhea with villous atrophy Chronic hiccup Chronic intestinal failure Congenital enteropathy due to enteropeptidase deficiency Congenital enteropathy involving intestinal mucosa development Congenital intestinal disease due to an enzymatic defect Congenital intestinal transport defect Congenital lactase deficiency Congenital pancreatic cyst Congenital respiratory-biliary fistula Congenital sucrase-isomaltase deficiency Crigler-Najjar syndrome Cystinosis Dietary iron overload disease Dubin-Johnson syndrome Enteric anendocrinosis Eosinophilic esophagitis Eosinophilic gastroenteritis FTH1-related iron overload Familial hypercholanemia Familial intrahepatic cholestasis Fanconi-Bickel syndrome Follicular cholangitis and pancreatitis Fulminant viral hepatitis Galactosemia Gastric linitis plastica Glycogen storage disease due to glucose-6-phosphatase deficiency Glycogen storage disease due to glycogen branching enzyme deficiency Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency Glycogen storage disease due to liver glycogen phosphorylase deficiency Glycogen storage disease due to liver phosphorylase kinase deficiency Hepatic veno-occlusive disease Hepatic veno-occlusive disease-immunodeficiency syndrome Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 Hepatoportal sclerosis Hereditary chronic pancreatitis Hereditary fructose intolerance Hyperbiliverdinemia Idiopathic achalasia Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome Intestinal disease due to fat malabsorption Intestinal disease due to vitamin absorption anomaly Intestinal lymphangiectasia Intractable diarrhea of infancy Isolated biliary atresia Isolated polycystic liver disease Low phospholipid-associated cholelithiasis Malakoplakia Mitochondrial DNA depletion syndrome, hepatocerebrorenal form Neonatal hemochromatosis Neonatal ichthyosis-sclerosing cholangitis syndrome Neonatal inflammatory skin and bowel disease Non-hypoproteinemic hypertrophic gastropathy Pancreatic insufficiency-anemia-hyperostosis syndrome Peroxisome biogenesis disorder Plummer-Vinson syndrome PrP systemic amyloidosis Primary biliary cholangitis Primary sclerosing cholangitis Primitive portal vein thrombosis Radiation proctitis Rare gastroesophageal disease Rare hereditary hemochromatosis Rare inflammatory bowel disease Rare metabolic liver disease Rare pancreatic disease Rare parenchymal liver disease Rare vascular liver disease Recurrent acute pancreatitis Reynolds syndrome Rotor syndrome Sandifer syndrome Severe immune-mediated enteropathy Short bowel syndrome Solitary rectal ulcer syndrome Steroid dehydrogenase deficiency-dental anomalies syndrome Syndromic diarrhea Transient familial neonatal hyperbilirubinemia Trehalase deficiency Tyrosinemia type 1 Undetermined colitis Whipple disease Wilson disease Zollinger-Ellison syndrome