Chest pain

Symptom Information:

Symptom ID: HPO:0100749
Chest pain (finding) [Orphanet:33050]
Chest Pain [Orphanet:33050]
Chest pain [OMIM:Chest pain]
Thoracic/chest pain [Orphanet:33050]
Chest pain [Orphanet:33050]
Chest pain [MedDRA:10008479]
Ache across chest [MedDRA:10008479]
Chest ache [MedDRA:10008479]
Chest aching [MedDRA:10008479]
Chest aching of [MedDRA:10008479]
Chest burning [MedDRA:10008479]
Chest burning pain of [MedDRA:10008479]
Chest distress [MedDRA:10008479]
Chest pain NEC [MedDRA:10008479]
Chest pain precordial [MedDRA:10008479]
Chest pain substernal [MedDRA:10008479]
Chest pain-L arm [MedDRA:10008479]
Generalised chest pain [MedDRA:10008479]
Generalised chest pains [MedDRA:10008479]
Nonspecific chest pain [MedDRA:10008479]
Other chest pain [MedDRA:10008479]
Pain chest [MedDRA:10008479]
Pain chest substernal [MedDRA:10008479]
Pain precordial [MedDRA:10008479]
Pain retrosternal [MedDRA:10008479]
Pain substernal [MedDRA:10008479]
Parasternal pain (excl organic) [MedDRA:10008479]
Precordial pain [MedDRA:10008479]
Retrosternal chest pain [MedDRA:10008479]
Retrosternal pain [MedDRA:10008479]
Substernal chest pain [MedDRA:10008479]
Substernal pain [MedDRA:10008479]
Thoracic pain [MedDRA:10008479]
Thorax pain [MedDRA:10008479]
Unspecified chest pain [MedDRA:10008479]
Chest pain aggravated [MedDRA:10008479]
Sternal pain [MedDRA:10008479]
Chest pain with radiation to left arm [MedDRA:10008479]
Chest pain exertional [MedDRA:10008479]
Generalized chest pain [MedDRA:10008479]
Chronic chest pain [MedDRA:10008479]
Acute chest pain [MedDRA:10008479]
Thoracalgia [MedDRA:10008479]
Precordial catch syndrome [MedDRA:10008479]
Chest pain (more common in male patients) [OMIM:Chest pain (more common in male patients)]
Thoracic pain [OMIM:Thoracic pain]
Cross references:
Orphanet:33050 "Thoracic/chest pain" [Orphanet:33050]
OMIM: "Chest pain" [OMIM:Chest pain]
OMIM: "Chest pain (more common in male patients)" [OMIM:Chest pain (more common in male patients)]
OMIM: "Thoracic pain" [OMIM:Thoracic pain]
UMLS:C0008031 "Chest Pain" [Orphanet:33050]
Is a (Direct Parents):
Orphanet Abnormality of the respiratory system
HPO         Abnormality of the thorax
MedDRA Pain and discomfort NEC
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the thorax(HPO:0000765)
                   Chest pain(HPO:0100749)
General disorders and administration site conditions(MedDRA:10018065)
    General system disorders NEC(MedDRA:10018073)
       Pain and discomfort NEC(MedDRA:10033372)
          Chest pain(HPO:0100749)
Database Frequency: 92 / 7739

All diseases associated with this symptom:

Acetazolamide-responsive myotonia (Orphanet:99736)
Adult heart tumor (Orphanet:874)
Adult pulmonary Langerhans cell histiocytosis (Orphanet:99874)
Alveolar echinococcosis (Orphanet:284)
Anti-glomerular basement membrane disease (Orphanet:375)
Antisynthetase syndrome (Orphanet:81)
Arrhythmogenic right ventricular dysplasia, familial, 10 (OMIM:610193)
Arrhythmogenic right ventricular dysplasia, familial, 5 (OMIM:604400)
Atrial tachyarrhythmia with short PR interval (Orphanet:844)
Brugada syndrome (Orphanet:130)
Cardiomyopathy, dilated, 3B (OMIM:302045)
Cardiomyopathy, familial hypertrophic, 1 (OMIM:192600)
Cardiomyopathy, familial hypertrophic, 13 (OMIM:613243)
Cardiomyopathy, familial hypertrophic, 14 (OMIM:613251)
Cardiomyopathy, familial hypertrophic, 18 (OMIM:613874)
Cardiomyopathy, familial hypertrophic, 2 (OMIM:115195)
Cardiomyopathy, familial hypertrophic, 4 (OMIM:115197)
Cardiomyopathy, familial hypertrophic, 6 (OMIM:600858)
Cardiomyopathy, familial hypertrophic, 7 (OMIM:613690)
Castleman disease (Orphanet:160)
Catecholaminergic polymorphic ventricular tachycardia (Orphanet:3286)
Combined pulmonary fibrosis-emphysema syndrome (Orphanet:300564)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Cryptogenic organizing pneumonia (Orphanet:1302)
Desmoid tumor (Orphanet:873)
Desquamative interstitial pneumonia (Orphanet:98852)
Ebola hemorrhagic fever (Orphanet:319218)
Ebstein malformation (Orphanet:1880)
Eosinophilic granuloma (Orphanet:99871)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Esophageal adenocarcinoma (Orphanet:99976)
Esophageal carcinoma (Orphanet:70482)
Esophageal squamous cell carcinoma (Orphanet:99977)
Essential thrombocythemia (Orphanet:3318)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Familial isolated hypertrophic cardiomyopathy (Orphanet:155)
Familial sick sinus syndrome (Orphanet:166282)
Familial thrombocytosis (Orphanet:71493)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Granulomatosis with polyangiitis (Orphanet:900)
Hemochromatosis, type 2A (OMIM:602390)
Hodgkin lymphoma (Orphanet:98293)
Hodgkin lymphoma, classical (Orphanet:391)
Hughes-Stovin syndrome (Orphanet:228116)
Hyperkalemic periodic paralysis (Orphanet:682)
Idiopathic acute eosinophilic pneumonia (Orphanet:724)
Idiopathic giant cell myocarditis (Orphanet:329874)
Idiopathic pulmonary alveolar proteinosis (Orphanet:747)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Idiopathic recurrent pericarditis (Orphanet:251307)
Lassa fever (Orphanet:99824)
Legionellosis (Orphanet:549)
Lymphangioleiomyomatosis (Orphanet:538)
Lymphoid interstitial pneumonia (Orphanet:79128)
Malakoplakia (Orphanet:556)
Malignant atrophic papulosis (Orphanet:679)
Marburg hemorrhagic fever (Orphanet:99826)
Marfan syndrome (Orphanet:558)
Mixed connective tissue disease (Orphanet:809)
Mulibrey nanism (Orphanet:2576)
Myotonia fluctuans (Orphanet:99734)
Myotonia permanens (Orphanet:99735)
Non-specific interstitial pneumonia (Orphanet:91364)
PGM1-CDG (Orphanet:319646)
Peripartum cardiomyopathy (Orphanet:563)
Porphyria (Orphanet:738)
Potassium-aggravated myotonia (Orphanet:612)
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome (Orphanet:228012)
Pulmonary arterial hypertension (Orphanet:182090)
Pulmonary blastoma (Orphanet:64741)
Pulmonary capillary hemangiomatosis (Orphanet:199241)
Pulmonary venoocclusive disease (Orphanet:31837)
Rheumatic fever (Orphanet:3099)
SAPHO syndrome (Orphanet:793)
Sarcoidosis (Orphanet:797)
Scleroderma (Orphanet:801)
Senile systemic amyloidosis (Orphanet:330001)
Sino-auricular heart block (Orphanet:1260)
Systemic sclerosis (Orphanet:90291)
TRAPS syndrome (Orphanet:32960)
Takayasu arteritis (Orphanet:3287)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Thymic carcinoma (Orphanet:99868)
Thymic epithelial neoplasm (Orphanet:3398)
Thymic tumor (Orphanet:100100)
Thymoma (Orphanet:99867)
Viral hemorrhagic fever (Orphanet:341)
Whipple disease (Orphanet:3452)
Wiskott-Aldrich syndrome (Orphanet:906)
Yellow fever (Orphanet:99829)