Esophageal varix
Symptom Information:
Symptom ID: | HPO:0002040 | |||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the gastrointestinal tract(HPO:0011024) Abnormality of the esophagus(HPO:0002031) Esophageal varix(HPO:0002040) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal vascular conditions(MedDRA:10018031) Esophageal varix(HPO:0002040) |
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Database Frequency: | 23 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ADAMS-OLIVER SYNDROME 5 | (OMIM:616028) |
Adams-Oliver syndrome | (Orphanet:974) |
Alström syndrome | (Orphanet:64) |
Alveolar echinococcosis | (Orphanet:284) |
Autosomal recessive polycystic kidney disease | (Orphanet:731) |
Budd-Chiari syndrome | (Orphanet:131) |
Caroli disease | (Orphanet:53035) |
Cholesteryl ester storage disease | (Orphanet:75234) |
Classical homocystinuria | (Orphanet:394) |
Early-onset familial noncirrhotic portal hypertension | (ORPHA:494348) |
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form | (Orphanet:308712) |
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form | (Orphanet:308684) |
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form | (Orphanet:308698) |
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form | (Orphanet:308670) |
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form | (Orphanet:308655) |
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form | (Orphanet:308638) |
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form | (Orphanet:308621) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
Hydatidosis | (Orphanet:400) |
Idiopathic copper-associated cirrhosis | (Orphanet:209919) |
Lysosomal acid lipase deficiency | (Orphanet:275761) |
Wilson disease | (Orphanet:905) |
Wolman disease | (Orphanet:75233) |