SE-ATLAS

Amylose systémique PrP Syndrome de dérèglement immunitaire-maladie inflammatoire de l'intestin-arthrite-infections récurrentes Gastro-entérite à éosinophiles Entéropathie congénitale due à un déficit de l'entéropeptidase Syndrome d'aplasie cutanée congénitale-lymphangiectasie intestinale Syndrome de diarrhée chronique-atrophie villositaire Cholangite sclérosante primitive Thrombose portale primitive Hémochromatose néonatale Syndrome d'entéropathie et endocrinopathie auto-immunes-susceptibilité aux infections chroniques Syndrome de Fanconi-Bickel Maladie de Whipple Diarrhée intraitable de l'enfant Déplétion de l'ADN mitochondrial, forme hépato-cérébro-rénale Diarrhée syndromique Polykystose rénale autosomique dominante Polykystose rénale autosomique récessive Maladie gastro-oesophagienne rare Cholangite biliaire primitive Maladie hépatique vasculaire rare Syndrome d'Alagille CADDS Maladie pancréatique rare Maladie métabolique hépatique rare Syndrome de l'ulcère solitaire du rectum Maladie rare du parenchyme hépatique 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 Enteropathie, autoimmune, Typ 2 Kolitis, unbestimmte Autoimmun-Pankreatitis Pankreatitis, chronische hereditäre Transiente neonatale Hyperbilirubinämie, familiäre Form Budd-Chiari-Syndrom Fistel, broncho-biliäre kongenitale Glykogenose durch Leber- und Muskel-Phosphorylasekinase-Mangel Biliäre Atresie-Milzfehlbildung-Syndrom Ösophagitis, eosinophile Cholestase, intrahepatische, familiäre Form Malakoplasie Virushepatitis, fulminante Anendokrinose, enterische Lebervenen-Verschlusskrankheit - Immunschwäche Cystinose Linitis plastica Plummer-Vinson-Syndrom