Deutsch
Clinical AreaGastroenterology
Associated diseases
- 5-FU toxicity
- Alagille syndrome, differential diagnosis
- Amyloidosis, differential diagnosis
- Angioedema, hereditary, differential diagnosis
- Anorectal malformations, [non-]syndromic; differential diagnosis
- Anorectal malformations, differential diagnosis
- ATP8B1 deficiency, differential diagnosis
- Cancer susceptibility upper gastrointestinal tract
- Cholestasis, congenital + adult; differential diagnosis
- Cholestasis, intrahepatic, pregnancy; differential diagnosis
- Cholestasis, progressive familial intrahepatic; differential diagnosis
- Citrin deficiency, neonatal intrahepatic cholestasis; differential diagnosis
- Colon cancer, hereditary non-polyposis; differential diagnosis
- Colon carcinoma, POLD1-related
- Colorectal cancers, hereditary; differential diagnosis
- Cowden syndrome, differential diagnosis
- Crigler-Najjar syndrome type I, unconjugated hyperbilirubinemia
- Crigler-Najjar syndrome type II, unconjugated hyperbilirubinemia
- Cystic fibrosis - full sequence
- Cystic fibrosis, most frequent mutations
- Cystische Fibrose, Differentialdiagnose
- Cytochrome P450 inherited disoders, differential diagnosis
- Deoxyguanosine Kinase Deficiency, mtDNA depletions syndrome, hepatocerebral; differential diagnosis
- Diaphragmatic hernias, congenital, differential diagnosis
- Ductal plate malformations, differential diagnosis
- Epidermolysis bullosa simplex with pyloric atresia, differential diagnosis
- Esophageal squamous cell cancer [susceptibility]
- Esophagus atresia/tracheo-esophageal fistulas, differential diagnosis
- Familial mediterranean fever
- Fanconi-Bickel syndrome
- Feingold syndrome 1
- Fructose-1,6-biphosphatase deficiency, differential diagnosis
- Gastric cancer, hereditary diffuse; in part multifactorial; differential diagnosis
- Gastroenterologic epithelial barrier disorders
- Gastroenterologic neuromuscular disorders, differential diagnosis
- Gastrointestinal tumors, monogeneic; differential diagnosis
- Gilbert [Meulengracht] syndrome, unconjugated hyperbilirubinemia
- Gilbert syndrome, unconjugated hyperbilirubinemia
- GM1-Gangliosidosis typ I-II, differential diagnosis
- GM1-Gangliosidosis type III, differential diagnosis
- Hamartomas [extra-gastrointestinal], differential diagnosis
- Head and neck cancer, susceptibility
- Hepatic lipase deficiency
- Hermansky-Pudlak syndrome, differential diagnosis
- Inflammatory bowel diseases + infantile enterocolitis, monogenic; DD
- Intestinal failure / Diarrhea, differential diagnosis
- Juvenile hemochromatosis [type 2], differential diagnosis
- Kolonkarzinom, POLE related
- Lactose intolerance, primary
- Lipoidproteinosis, differential diagnosis
- Meckel[-Gruber] syndrome, differential diagnosis
- MIRAGE syndrome, differential diagnosis
- Mitochondrial liver diseases, difrferential diagnosis
- Morbus Crohn, genetic predisposition
- Morbus Hirschsprung, familial; differential diagnosis
- Morbus Hirschsprung, syndromic; differential diagnosis
- Morbus Niemann-Pick, type C; differential diagnosis
- Morbus Wolman, differential diagnosis
- Mowat-Wilson syndrome; differential diagnosis
- Multiple endocrine tumors, differential diagnosis
- Myhre syndrome, differential diagnosis
- Neuroendocrine tumors/polyposis, pediatric; differential diagnosis
- Omphalocele, laparoschisis; differential diagnosis
- Pancreatic cancer [familial cancer syndromes]
- Pancreatic cancer [susceptibility loci]
- Pancreatic cancer, after chronic pancreatitis; differential diagnosis
- Pancreatitis, chronic; differential diagnosis
- Pankreas-Karzinom - PARP-Inhibitor-Therapie
- Paraganglioma / pheochromocytoma, differential diagnosis
- Paraganglioma 1 / phaeochromocytoma
- Paraganglioma 3 / phaeochromocytoma
- Paraganglioma 4 / phaeochromocytoma
- Peutz-Jeghers syndrome
- Polycystic liver disease, differential diagnosis
- Polyposis coli, differential diagnosis
- Polyposis syndrome, juvenile
- Polyposis syndrome, serrated; differential diagnosis
- Polyposis, APC-assoiated, differential diagnosis
- Polyposis, familial adenomatous 3
- Polyposis, familial adenomatous 4
- Polyposis, familial adenomatous; FAP
- Polyposis, MUTYH associated
- Polyps, hamartomatous [gastrointestinal], differential diagnosis
- Porphyria, differential diagnosis
- Porphyria, erythropoetic 1
- PTEN hamartoma tumor syndrome
- Rotor syndrome, differential diagnosis
- Short bowel syndrome, congenital
- Signet ring cell carcinoma, gastric; differential diagnosis
- Stomach cancer, predisposition
- Sulfatase deficiency, multiple
- Sulfatase deficiency, multiple; differential diagnosis
- Tricho-hepato-enteric syndrome, differential diagnosis
- Tumor predisposition syndrome, BAP1-dependent
- Tumour intersecting set panel
- Tyrosinaemia type I-III, differential diagnosis
Notes on the clinical area
Here you will find the disease-related gene panels available for the clinical area specified above.
If you cannot find the disease you are looking for, please use a known synonym in the search (also in English).