Pulmonary hypertension

Symptom Information:

Symptom ID: HPO:0002092
Synonyms:
PRIMARY PULMONARY HYPERTENSION [HPO:0002092]
PULMONARY ARTERIAL HYPERTENSION [HPO:0002092]
Pulmonary artery hypertension [HPO:0002092]
Pulmonary hypertension (disorder) [Orphanet:33650]
Pulmonary arterial hypertension [Orphanet:33650]
Pulmonary Hypertension [Orphanet:33650]
Primary pulmonary hypertension [OMIM:Primary pulmonary hypertension]
Pulmonary arterial hypertension [OMIM:Pulmonary arterial hypertension]
Pulmonary artery hypertension [OMIM:Pulmonary artery hypertension]
Pulmonary hypertension [OMIM:Pulmonary hypertension]
Pulmonary hypertension [Orphanet:33650]
Pulmonary hypertension [MedDRA:10037400]
Hypertension pulmonary [MedDRA:10037400]
Pulmonary hypertension aggravated [MedDRA:10037400]
Pulmonary hypertension NOS [MedDRA:10037400]
Pulmonary hypertension NOS aggravated [MedDRA:10037400]
Pulmonary hypertension secondary [MedDRA:10037400]
Hypertension pulmonary aggravated [MedDRA:10037400]
Chronic thromboembolic pulmonary hypertension [MedDRA:10037400]
CTEPH [MedDRA:10037400]
Pulmonary arterial hypertension [MedDRA:10064911]
Primary pulmonary hypertension [MedDRA:10064911]
Pulmonary hypertension primary [MedDRA:10064911]
Associated with (APAH) [MedDRA:10064911]
Idiopathic (IPAH) [MedDRA:10064911]
Familial (FPAH) [MedDRA:10064911]
Associated with pulmonary arterial hypertension [MedDRA:10064911]
Idiopathic pulmonary arterial hypertension [MedDRA:10064911]
Familial pulmonary arterial hypertension [MedDRA:10064911]
Secondary pulmonary arterial hypertension [MedDRA:10064911]
'Primary' pulmonary hypertension [OMIM:'Primary' pulmonary hypertension]
Pulmonary arterial hypertension (in 3 patients) [OMIM:Pulmonary arterial hypertension (in 3 patients)]
Pulmonary artery hypertension (in one patient) [OMIM:Pulmonary artery hypertension (in one patient)]
Pulmonary artery hypertension (in some patients) [OMIM:Pulmonary artery hypertension (in some patients)]
Pulmonary hypertension (1 patient) [OMIM:Pulmonary hypertension (1 patient)]
Pulmonary hypertension (1/4 patients) [OMIM:Pulmonary hypertension (1/4 patients)]
Pulmonary hypertension (neonatal period) [OMIM:Pulmonary hypertension (neonatal period)]
Pulmonary hypertension (secondary to scoliosis, in some patients) [OMIM:Pulmonary hypertension (secondary to scoliosis, in some patients)]
Pulmonary hypertensions [MedDRA:10037401]
]Pulmonary hypertension, severe (in end-stage disease) [OMIM,cm]
Quality:
Cross references:
Orphanet:33650 "Pulmonary hypertension" [Orphanet:33650]
OMIM: "Primary pulmonary hypertension" [OMIM:Primary pulmonary hypertension]
OMIM: "Pulmonary arterial hypertension" [OMIM:Pulmonary arterial hypertension]
OMIM: "Pulmonary artery hypertension" [OMIM:Pulmonary artery hypertension]
OMIM: "Pulmonary hypertension" [OMIM:Pulmonary hypertension]
OMIM: "'Primary' pulmonary hypertension" [OMIM:'Primary' pulmonary hypertension]
OMIM: "Pulmonary arterial hypertension (in 3 patients)" [OMIM:Pulmonary arterial hypertension (in 3 patients)]
OMIM: "Pulmonary artery hypertension (in one patient)" [OMIM:Pulmonary artery hypertension (in one patient)]
OMIM: "Pulmonary artery hypertension (in some patients)" [OMIM:Pulmonary artery hypertension (in some patients)]
OMIM: "Pulmonary hypertension (1 patient)" [OMIM:Pulmonary hypertension (1 patient)]
OMIM: "Pulmonary hypertension (1/4 patients)" [OMIM:Pulmonary hypertension (1/4 patients)]
OMIM: "Pulmonary hypertension (neonatal period)" [OMIM:Pulmonary hypertension (neonatal period)]
OMIM: "Pulmonary hypertension (secondary to scoliosis, in some patients)" [OMIM:Pulmonary hypertension (secondary to scoliosis, in some patients)]
UMLS:C2973725 "Pulmonary arterial hypertension" [Orphanet:33650]
UMLS:C0020542 "Pulmonary Hypertension" [Orphanet:33650]
Is a (Direct Parents):
MedDRA Vascular hypertensive disorders
HPO         Abnormality of lung morphology
HPO         Elevated pulmonary artery pressure
Orphanet Abnormality of the respiratory system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of lung morphology(HPO:0002088)
                Pulmonary hypertension(HPO:0002092)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular hypertensive disorders(MedDRA:10057166)
       Pulmonary hypertension(HPO:0002092)
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)