SE-ATLAS

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