Dyspnea

Symptom Information:

Symptom ID: HPO:0002094
Synonyms:
Shortness of breath [HPO:0002094]
Dyspnea (finding) [Orphanet:33100]
Difficulty breathing (finding) [Orphanet:33100]
dyspnea [HPO:0002094]
Dyspnea [Orphanet:33100]
Dyspnea [OMIM:Dyspnea]
Shortness of breath [OMIM:Shortness of breath]
Respiratory distress/dyspnea/respiratory failure/lung volume reduction [Orphanet:33100]
Dyspnoea [Orphanet:33100]
Dyspnoea [MedDRA:10013968]
Air hunger [MedDRA:10013968]
Breath shortness [MedDRA:10013968]
Breathing difficult [MedDRA:10013968]
Breathlessness [MedDRA:10013968]
Difficulty breathing [MedDRA:10013968]
Dyspnea [MedDRA:10013968]
Dyspnea and respiratory abnormalities [MedDRA:10013968]
Dyspnea exacerbated [MedDRA:10013968]
Dyspnoea exacerbated [MedDRA:10013968]
Dyspnoea NOS [MedDRA:10013968]
Gasping [MedDRA:10013968]
Hunger air [MedDRA:10013968]
Increased shortness of breath [MedDRA:10013968]
Increased SOB [MedDRA:10013968]
Increased work of breathing [MedDRA:10013968]
Labored breathing [MedDRA:10013968]
Laboured breathing [MedDRA:10013968]
Laboured respiration [MedDRA:10013968]
Marked inactivity of chest wall on inspiratory effort [MedDRA:10013968]
Other dyspnea and respiratory abnormality [MedDRA:10013968]
Respiration labored [MedDRA:10013968]
Respiration laboured [MedDRA:10013968]
Respiratory tract closed sensation of [MedDRA:10013968]
Short of breath [MedDRA:10013968]
Shortness of breath [MedDRA:10013968]
SOB [MedDRA:10013968]
SOB (shortness of breath) [MedDRA:10013968]
Labored respiration [MedDRA:10013968]
Acute dyspnea [MedDRA:10013968]
Acute dyspnoea [MedDRA:10013968]
Dyspnea (1 patient) [OMIM:Dyspnea (1 patient)]
Dyspnea (onset 35 years in smokers, 45 years in nonsmokers) [OMIM:Dyspnea (onset 35 years in smokers, 45 years in nonsmokers)]
Lung volume reduction [Orphanet:33100]
Dyspnoeas [MedDRA:10013975]
Quality:
Cross references:
Orphanet:33100 "Respiratory distress/dyspnea/respiratory failure/lung volume reduction" [Orphanet:33100]
OMIM: "Dyspnea" [OMIM:Dyspnea]
OMIM: "Shortness of breath" [OMIM:Shortness of breath]
OMIM: "Dyspnea (1 patient)" [OMIM:Dyspnea (1 patient)]
OMIM: "Dyspnea (onset 35 years in smokers, 45 years in nonsmokers)" [OMIM:Dyspnea (onset 35 years in smokers, 45 years in nonsmokers)]
UMLS:C2024878 "dyspnea" [HPO:0002094]
UMLS:C0013404 "Dyspnea" [Orphanet:33100]
Is a (Direct Parents):
HPO         Paroxysmal dyspnea
HPO         Respiratory insufficiency
Orphanet Abnormality of the respiratory system
MedDRA Cardiac disorder signs and symptoms
Orphanet Respiratory insufficiency
HPO         Orthopnea
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)
                Respiratory insufficiency(HPO:0002093)
                   Dyspnea(HPO:0002094)
          Functional respiratory abnormality(HPO:0002795)
             Respiratory insufficiency(HPO:0002093)
                Dyspnea(HPO:0002094)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Cardiac disorder signs and symptoms(MedDRA:10007539)
       Dyspnea(HPO:0002094)
Database Frequency: 132 / 7739
Resource:

All diseases associated with this symptom:

Acute interstitial pneumonia (Orphanet:79126)
Alpha-1-antitrypsin deficiency (Orphanet:60)
Alström syndrome (Orphanet:64)
Anti-glomerular basement membrane disease (Orphanet:375)
Arrhythmogenic right ventricular dysplasia, familial, 10 (OMIM:610193)
Arrhythmogenic right ventricular dysplasia, familial, 11 (OMIM:610476)
Arrhythmogenic right ventricular dysplasia, familial, 6 (OMIM:604401)
Atrial standstill (Orphanet:1344)
Atrial tachyarrhythmia with short PR interval (Orphanet:844)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
Bronchiolitis obliterans with obstructive pulmonary disease (Orphanet:1303)
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS (OMIM:606842)
COLD-INDUCED SWEATING SYNDROME 1 (OMIM:272430)
CYANOSIS AND HEPATIC DISEASE (OMIM:219400)
Carbamoylphosphate synthetase deficiency (Orphanet:147)
Cardiomyopathy, dilated, 1BB (OMIM:612877)
Cardiomyopathy, dilated, 1D (OMIM:601494)
Cardiomyopathy, dilated, 1M (OMIM:607482)
Cardiomyopathy, dilated, 1Q (OMIM:609915)
Cardiomyopathy, dilated, 1W (OMIM:611407)
Cardiomyopathy, dilated, 1X (OMIM:611615)
Cardiomyopathy, dilated, 1Y (OMIM:611878)
Cardiomyopathy, dilated, 1Z (OMIM:611879)
Cardiomyopathy, dilated, 2A (OMIM:611880)
Cardiomyopathy, familial hypertrophic, 1 (OMIM:192600)
Cardiomyopathy, familial hypertrophic, 12 (OMIM:612124)
Cardiomyopathy, familial hypertrophic, 13 (OMIM:613243)
Cardiomyopathy, familial hypertrophic, 14 (OMIM:613251)
Cardiomyopathy, familial hypertrophic, 15 (OMIM:613255)
Cardiomyopathy, familial hypertrophic, 16 (OMIM:613838)
Cardiomyopathy, familial hypertrophic, 17 (OMIM:613873)
Cardiomyopathy, familial hypertrophic, 2 (OMIM:115195)
Cardiomyopathy, familial hypertrophic, 3 (OMIM:115196)
Cardiomyopathy, familial hypertrophic, 4 (OMIM:115197)
Cardiomyopathy, familial hypertrophic, 7 (OMIM:613690)
Cardiomyopathy, familial restrictive 2 (OMIM:609578)
Cardiomyopathy, familial restrictive, 1 (OMIM:115210)
Cardiomyopathy, hypertrophic, 25 (OMIM:607487)
Chronic respiratory distress with surfactant metabolism deficiency (Orphanet:217566)
Cold-induced sweating syndrome (Orphanet:157820)
Combined oxidative phosphorylation defect type 9 (Orphanet:319509)
Combined pulmonary fibrosis-emphysema syndrome (Orphanet:300564)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Cryptogenic organizing pneumonia (Orphanet:1302)
D,L-2-hydroxyglutaric aciduria (Orphanet:356978)
Desquamative interstitial pneumonia (Orphanet:98852)
Early infantile epileptic encephalopathy (Orphanet:1934)
Fabry disease (Orphanet:324)
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease (Orphanet:436242)
Familial isolated dilated cardiomyopathy (Orphanet:154)
Familial isolated restrictive cardiomyopathy (Orphanet:75249)
Familial progressive cardiac conduction defect (Orphanet:871)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
Fructose-1,6-bisphosphatase deficiency (Orphanet:348)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
Hemochromatosis, type 2A (OMIM:602390)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hereditary myopathy with lactic acidosis due to ISCU deficiency (Orphanet:43115)
Heritable pulmonary arterial hypertension (Orphanet:275777)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
Hurler syndrome (Orphanet:93473)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation (Orphanet:324525)
INFANTILE LIVER FAILURE SYNDROME 2 (OMIM:615486)
Idiopathic and/or familial pulmonary arterial hypertension (Orphanet:422)
Idiopathic giant cell myocarditis (Orphanet:329874)
Idiopathic pulmonary alveolar proteinosis (Orphanet:747)
Idiopathic pulmonary arterial hypertension (Orphanet:275766)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Idiopathic recurrent pericarditis (Orphanet:251307)
Infant acute respiratory distress syndrome (Orphanet:70587)
Infantile epileptic-dyskinetic encephalopathy (Orphanet:364063)
Joubert syndrome 1 (OMIM:213300)
Joubert syndrome 21 (OMIM:615636)
Joubert syndrome with oculorenal defect (Orphanet:2318)
LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY (OMIM:606183)
LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME (OMIM:308940)
Left ventricular noncompaction 10 (OMIM:615396)
Leigh syndrome (Orphanet:506)
Letterer-Siwe disease (Orphanet:99870)
Lymphangioleiomyomatosis (Orphanet:538)
Lymphoid interstitial pneumonia (Orphanet:79128)
MEIER-GORLIN SYNDROME 3 (OMIM:613803)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
Maple syrup urine disease (Orphanet:511)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Mulibrey nanism (Orphanet:2576)
Multifocal atrial tachycardia (Orphanet:3282)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Naxos disease (Orphanet:34217)
Neonatal acute respiratory distress with surfactant metabolism deficiency (Orphanet:217563)
Neonatal severe primary hyperparathyroidism (Orphanet:417)
Nephronophthisis 1 (OMIM:256100)
Niemann-Pick disease type B (Orphanet:77293)
Niemann-Pick disease type E (Orphanet:99022)
Non-specific interstitial pneumonia (Orphanet:91364)
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2 (OMIM:615399)
PGM1-CDG (Orphanet:319646)
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA (OMIM:113900)
PULMONARY HYPERTENSION, PRIMARY, 1 (OMIM:178600)
PULMONARY HYPERTENSION, PRIMARY, 3 (OMIM:615343)
Pediatric systemic sclerosis (Orphanet:93567)
Peripartum cardiomyopathy (Orphanet:563)
Progressive external ophthalmoplegia - myopathy - emaciation (Orphanet:352447)
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome (Orphanet:228012)
Pulmonary capillary hemangiomatosis (Orphanet:199241)
Pulmonary venoocclusive disease (Orphanet:31837)
Respiratory bronchiolitis - interstitial lung disease (Orphanet:79127)
Riboflavin transporter deficiency (Orphanet:97229)
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 (OMIM:181000)
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1 (OMIM:265120)
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3 (OMIM:610921)
SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5 (OMIM:614370)
Sarcoidosis (Orphanet:797)
Senile systemic amyloidosis (Orphanet:330001)
Sino-auricular heart block (Orphanet:1260)
Spasticity - intellectual deficit - X-linked epilepsy (Orphanet:3175)
Steinert myotonic dystrophy (Orphanet:273)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 (OMIM:610655)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Tracheobronchopathia osteochondroplastica (Orphanet:3348)
Uhl anomaly (Orphanet:3403)
Wolfram syndrome (Orphanet:3463)