Esophageal varix

Symptom Information:

Symptom ID: HPO:0002040
Synonyms:
Esophageal varices (disorder) [Orphanet:27270]
Esophageal Varices [Orphanet:27270]
Esophageal varices [OMIM:Esophageal varices]
Esophageal varices [Orphanet:27270]
Varices oesophageal [HPO:0002040]
Varices oesophageal [Orphanet:27270]
Varices oesophageal [MedDRA:10056091]
Esophageal varices [MedDRA:10056091]
Esophageal varices in diseases classified elsewhere [MedDRA:10056091]
Esophageal varices in diseases classified elsewhere, without mention of bleeding [MedDRA:10056091]
Esophageal varices without mention of bleeding [MedDRA:10056091]
Oesophageal varices in cirrhosis of liver [MedDRA:10056091]
Oesophageal varices NOS [MedDRA:10056091]
Oesophageal varices without mention of bleeding [MedDRA:10056091]
Varices esophageal [MedDRA:10056091]
Esophageal varices in cirrhosis of liver [MedDRA:10056091]
Gastrooesophageal varices [MedDRA:10056091]
Gastroesophageal varices [MedDRA:10056091]
Oesophageal varices [MedDRA:10030209]
Quality:
Cross references:
Orphanet:27270 "Esophageal varices" [Orphanet:27270]
OMIM: "Esophageal varices" [OMIM:Esophageal varices]
UMLS:C0014867 "Esophageal Varices" [Orphanet:27270]
Is a (Direct Parents):
Orphanet Functional anomalies of the digestive system
MedDRA Gastrointestinal vascular conditions
HPO         Abnormality of the esophagus
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)
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)