Dyspnea
Symptom Information:
Symptom ID: | HPO:0002094 | ||||||||||||||||||||||||||||||||||||||||||||
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) Functional respiratory abnormality(HPO:0002795) Respiratory insufficiency(HPO:0002093) Dyspnea(HPO:0002094) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Respiratory insufficiency(HPO:0002093) Dyspnea(HPO:0002094) MedDRA: Cardiac disorders(MedDRA:10007541) Cardiac disorder signs and symptoms(MedDRA:10007539) Dyspnea(HPO:0002094) |
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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) |