Portal hypertension
Symptom Information:
Symptom ID: | HPO:0001409 | ||||||||||||
Synonyms: |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of cardiovascular system physiology(HPO:0011025) Hypertension(HPO:0000822) Portal hypertension(HPO:0001409) 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) MedDRA: Vascular disorders(MedDRA:10047065) Vascular hypertensive disorders(MedDRA:10057166) Portal hypertension(HPO:0001409) |
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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) |