Chest pain
Symptom Information:
Symptom ID: | HPO:0100749 | ||||||||||||||||||||||||||||||||||||||||||||||
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 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) MedDRA: General disorders and administration site conditions(MedDRA:10018065) General system disorders NEC(MedDRA:10018073) Pain and discomfort NEC(MedDRA:10033372) Chest pain(HPO:0100749) |
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Database Frequency: | 92 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
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) |
FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT | (OMIM:134610) |
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) |