Portal hypertension

Symptom Information:

Symptom ID: HPO:0001409
Synonyms:
Portal hypertension (disorder) [Orphanet:29720]
Hypertension, Portal [Orphanet:29720]
Portal hypertension [OMIM:Portal hypertension]
Portal hypertension [Orphanet:29720]
Portal hypertension [MedDRA:10036200]
Hypertension portal [MedDRA:10036200]
Prehepatic portal hypertension [MedDRA:10036200]
Cruveilhier-Baumgarten syndrome [MedDRA:10036200]
Non-cirrhotic portal fibrosis [MedDRA:10036200]
Idiopathic portal hypertension [MedDRA:10036200]
Portal hypertension (in some patients) [OMIM:Portal hypertension (in some patients)]
Portal hypertensions [MedDRA:10036201]
Quality:
Cross references:
Orphanet:29720 "Portal hypertension" [Orphanet:29720]
OMIM: "Portal hypertension" [OMIM:Portal hypertension]
OMIM: "Portal hypertension (in some patients)" [OMIM:Portal hypertension (in some patients)]
UMLS:C0020541 "Hypertension, Portal" [Orphanet:29720]
Is a (Direct Parents):
HPO         Hypertension
HPO         Abnormality of the hepatic vasculature
Orphanet Decreased liver function
MedDRA Vascular hypertensive disorders
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 liver(HPO:0001392)
                Abnormality of the hepatic vasculature(HPO:0006707)
                   Portal hypertension(HPO:0001409)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of cardiovascular system physiology(HPO:0011025)
             Hypertension(HPO:0000822)
                Portal hypertension(HPO:0001409)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular hypertensive disorders(MedDRA:10057166)
       Portal hypertension(HPO:0001409)
Database Frequency: 39 / 7739
Resource:

All diseases associated with this symptom:

Adams-Oliver syndrome (Orphanet:974)
Alström syndrome (Orphanet:64)
Alveolar echinococcosis (Orphanet:284)
Autosomal recessive polycystic kidney disease (Orphanet:731)
BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION (OMIM:210050)
Budd-Chiari syndrome (Orphanet:131)
CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4 (OMIM:615878)
Caroli disease (Orphanet:53035)
Cholestasis - lymphedema (Orphanet:1414)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Cirrhotic cardiomyopathy (Orphanet:57777)
Cystinosis (Orphanet:213)
Early-onset familial noncirrhotic portal hypertension (ORPHA:494348)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Glycogen storage disease due to glycogen branching enzyme deficiency (Orphanet:367)
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)
Hemochromatosis, type 2A (OMIM:602390)
Hereditary North American Indian childhood cirrhosis (Orphanet:168583)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hydatidosis (Orphanet:400)
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (Orphanet:83639)
Ichthyosis - hypotrichosis - sclerosing cholangitis (Orphanet:59303)
Idiopathic copper-associated cirrhosis (Orphanet:209919)
Joubert syndrome with hepatic defect (Orphanet:1454)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Neonatal hemochromatosis (Orphanet:446)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polycythemia vera (Orphanet:729)
Systemic mastocytosis (Orphanet:2467)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5 (OMIM:615506)
Williams syndrome (Orphanet:904)