Pulmonary hypertension
Symptom Information:
Symptom ID: | HPO:0002092 | ||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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 respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Pulmonary hypertension(HPO:0002092) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of the vasculature(HPO:0002597) Abnormality of the pulmonary vasculature(HPO:0004930) Abnormality of the pulmonary artery(HPO:0004414) Elevated pulmonary artery pressure(HPO:0004890) Pulmonary hypertension(HPO:0002092) MedDRA: Vascular disorders(MedDRA:10047065) Vascular hypertensive disorders(MedDRA:10057166) Pulmonary hypertension(HPO:0002092) |
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Database Frequency: | 109 / 7739 | ||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
ADAMS-OLIVER SYNDROME 1 | (OMIM:100300) |
ADAMS-OLIVER SYNDROME 5 | (OMIM:616028) |
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA | (OMIM:613623) |
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES | (OMIM:300887) |
ATRIAL SEPTAL DEFECT 9 | (OMIM:614475) |
ATRIOVENTRICULAR SEPTAL DEFECT 3 | (OMIM:600309) |
Acute interstitial pneumonia | (Orphanet:79126) |
Adams-Oliver syndrome | (Orphanet:974) |
Aldosterone-producing adenoma with seizures and neurological abnormalities | (Orphanet:369929) |
Allergic bronchopulmonary aspergillosis | (Orphanet:1164) |
Alström syndrome | (Orphanet:64) |
Antisynthetase syndrome | (Orphanet:81) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Atrial septal defect - atrioventricular conduction defects syndrome | (Orphanet:1479) |
Atrioventricular canal defect | (Orphanet:98722) |
Autosomal recessive malignant osteopetrosis | (Orphanet:667) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Beta-thalassemia intermedia | (Orphanet:231222) |
Beta-thalassemia major | (Orphanet:231214) |
Blau syndrome | (Orphanet:90340) |
Braddock syndrome | (Orphanet:52047) |
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 | (OMIM:617047) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22 | (OMIM:616045) |
CREST syndrome | (Orphanet:90290) |
Cardiomyopathy, dilated, 1R | (OMIM:613424) |
Cardiomyopathy, dilated, 1S | (OMIM:613426) |
Cardiomyopathy, familial hypertrophic, 15 | (OMIM:613255) |
Cardiomyopathy, familial hypertrophic, 8 | (OMIM:608751) |
Cholesteryl ester storage disease | (Orphanet:75234) |
Combined pulmonary fibrosis-emphysema syndrome | (Orphanet:300564) |
Congenital alveolar capillary dysplasia | (Orphanet:210122) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
Congenital total pulmonary venous return anomaly | (Orphanet:99125) |
Deafness - encephaloneuropathy - obesity - valvulopathy | (Orphanet:254898) |
Dermatomyositis | (Orphanet:221) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
Eosinophilic granuloma | (Orphanet:99871) |
Familial thrombocytosis | (Orphanet:71493) |
Fatal multiple mitochondrial dysfunction syndrome | (Orphanet:289573) |
GELEOPHYSIC DYSPLASIA 2 | (OMIM:614185) |
GLYCOGEN STORAGE DISEASE Ic | (OMIM:232240) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Geleophysic dysplasia | (Orphanet:2623) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
Heritable pulmonary arterial hypertension | (Orphanet:275777) |
Hughes-Stovin syndrome | (Orphanet:228116) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
Idiopathic and/or familial pulmonary arterial hypertension | (Orphanet:422) |
Idiopathic pulmonary arterial hypertension | (Orphanet:275766) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Incontinentia pigmenti | (Orphanet:464) |
KAGAMI-OGATA SYNDROME | (OMIM:608149) |
Keutel syndrome | (Orphanet:85202) |
Left ventricular noncompaction 8 | (OMIM:615373) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
Limited systemic sclerosis | (Orphanet:220407) |
Lymphedema - cerebral arteriovenous anomaly | (Orphanet:86914) |
Lysosomal acid lipase deficiency | (Orphanet:275761) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME | (OMIM:613834) |
Marshall-Smith syndrome | (Orphanet:561) |
Methylmalonic acidemia with homocystinuria, type cblJ | (Orphanet:369955) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mixed connective tissue disease | (Orphanet:809) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Neonatal acute respiratory distress with surfactant metabolism deficiency | (Orphanet:217563) |
Neonatal hemochromatosis | (Orphanet:446) |
Nestor-Guillermo progeria syndrome | (Orphanet:280576) |
OSTEOGENESIS IMPERFECTA, TYPE III | (OMIM:259420) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Osteogenesis imperfecta type 3 | (Orphanet:216812) |
PULMONARY HYPERTENSION, PRIMARY, 2 | (OMIM:615342) |
PULMONARY HYPERTENSION, PRIMARY, 3 | (OMIM:615343) |
PULMONARY HYPERTENSION, PRIMARY, 4 | (OMIM:615344) |
PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:265400) |
Patent arterial duct | (Orphanet:706) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
Pulmonary venoocclusive disease | (Orphanet:31837) |
ROWLEY-ROSENBERG SYNDROME | (OMIM:268500) |
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE | (OMIM:613320) |
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1 | (OMIM:265120) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Scleroderma | (Orphanet:801) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Systemic sclerosis | (Orphanet:90291) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
Takayasu arteritis | (Orphanet:3287) |
Timothy syndrome | (Orphanet:65283) |
Tropical endomyocardial fibrosis | (Orphanet:75565) |
Wolman disease | (Orphanet:75233) |
Yunis-Varon syndrome | (Orphanet:3472) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |