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Disease association ontology term - MONDO:0004335 - digestive system disorder

Term summary

ID
MONDO:0004335
Name
digestive system disorder
Ontology or CV name
Disease association
Definition
A disease or disorder that involves the digestive system.

Parents

Annotation

Disease association

MONDO:0013111 - acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins

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MONDO:0008294 - acute intermittent porphyria

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MONDO:0012730 - aortic aneurysm, familial thoracic 6

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MONDO:0000447 - autosomal dominant polycystic liver disease

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MONDO:0013662 - Barrett esophagus

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MONDO:0011559 - benign recurrent intrahepatic cholestasis type 2

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MONDO:0001751 - cholestasis

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MONDO:0013995 - cholestasis, intrahepatic, of pregnancy, 3

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MONDO:0030810 - cholestasis, progressive familial intrahepatic, 10

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MONDO:0031040 - cholestasis, progressive familial intrahepatic, 12

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MONDO:0000987 - cholesterolosis of gallbladder

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MONDO:0014528 - chronic atrial and intestinal dysrhythmia

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MONDO:0005575 - colorectal cancer

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MONDO:0014375 - congenital diarrhea 7 with exudative enteropathy

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MONDO:0008964 - congenital secretory chloride diarrhea 1

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MONDO:0009114 - congenital sucrase-isomaltase deficiency

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MONDO:0018794 - cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder

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MONDO:0005015 - diabetes mellitus

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MONDO:0014488 - diabetes mellitus, noninsulin-dependent, 5

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MONDO:0976266 - diarrhea 14, congenital

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MONDO:0958224 - encephalopathy, porphyria-related

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MONDO:0001676 - erythropoietic protoporphyria

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MONDO:0015278 - familial pancreatic carcinoma

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MONDO:0008296 - familial porphyria cutanea tarda

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MONDO:0010939 - gallbladder disease 1

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MONDO:0001056 - gastric cancer

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MONDO:0800030 - gastrointestinal defects and immunodeficiency syndrome 1

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MONDO:0030669 - gastrointestinal defects and immunodeficiency syndrome 2

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MONDO:0011719 - gastrointestinal stromal tumor

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MONDO:0002520 - hepatic porphyria

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MONDO:0007256 - hepatocellular carcinoma

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MONDO:0007369 - hereditary coproporphyria

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MONDO:0009238 - hereditary folate malabsorption

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MONDO:0018630 - hereditary nonpolyposis colon cancer

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MONDO:0011236 - hyperinsulinemic hypoglycemia, familial, 3

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MONDO:0011717 - hyperinsulinism-hyperammonemia syndrome

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MONDO:0024568 - infantile liver failure syndrome 1

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MONDO:0014659 - infantile liver failure syndrome 2

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MONDO:0032844 - infantile liver failure syndrome 3

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MONDO:0012610 - inflammatory bowel disease 10

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MONDO:0012831 - inflammatory bowel disease 13

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MONDO:0006065 - lactose intolerance adult type

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MONDO:0958226 - leukoencephalopathy, porphyria-related

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MONDO:0024477 - liver and intrahepatic bile duct neoplasm

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MONDO:0005835 - Lynch syndrome

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MONDO:0007356 - Lynch syndrome 1

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MONDO:0012249 - Lynch syndrome 2

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MONDO:0013699 - Lynch syndrome 4

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MONDO:0013710 - Lynch syndrome 5

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MONDO:0018911 - maturity-onset diabetes of the young

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MONDO:0014674 - maturity-onset diabetes of the young type 14

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MONDO:0007453 - maturity-onset diabetes of the young type 2

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MONDO:0025708 - megacystis-microcolon-intestinal hypoperistalsis syndrome 2

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MONDO:0030296 - megacystis-microcolon-intestinal hypoperistalsis syndrome 4

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MONDO:0030329 - megacystis-microcolon-intestinal hypoperistalsis syndrome 5

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MONDO:0009635 - microvillus inclusion disease

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MONDO:0015967 - monogenic diabetes

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MONDO:0013542 - Moyamoya disease 5

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MONDO:0008018 - Muir-Torre syndrome

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MONDO:0009465 - multiple intestinal atresia

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MONDO:0013452 - multisystemic smooth muscle dysfunction syndrome

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MONDO:0016391 - neonatal diabetes mellitus

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MONDO:0012992 - pancreatic insufficiency-anemia-hyperostosis syndrome

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MONDO:0100165 - permanent neonatal diabetes mellitus 1

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MONDO:0008265 - polycystic liver disease 1

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MONDO:0014860 - polycystic liver disease 2

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MONDO:0054743 - polycystic liver disease 3 with or without kidney cysts

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MONDO:0015104 - porphyria cutanea tarda

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MONDO:0013000 - porphyria due to ALA dehydratase deficiency

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MONDO:0011156 - progressive familial intrahepatic cholestasis type 2

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MONDO:0011214 - progressive familial intrahepatic cholestasis type 3

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MONDO:0008319 - protoporphyria, erythropoietic, 1

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MONDO:0013771 - transient infantile hypertriglyceridemia and hepatosteatosis

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MONDO:0009105 - trichohepatoenteric syndrome

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MONDO:0024541 - trichohepatoenteric syndrome 1

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MONDO:0013818 - trichohepatoenteric syndrome 2

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MONDO:0005148 - type 2 diabetes mellitus

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MONDO:0008297 - variegate porphyria

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MONDO:0957577 - variegate porphyria, childhood-onset

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MONDO:0020754 - visceral myopathy 1

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MONDO:0859157 - visceral myopathy 2

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MONDO:0010420 - X-linked erythropoietic protoporphyria

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