Syncope
Symptom Information:
Symptom ID: | HPO:0001279 | ||||
Synonyms: |
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Quality: | |||||
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 cardiovascular system(HPO:0001626) Abnormality of cardiovascular system physiology(HPO:0011025) Syncope(HPO:0001279) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Disturbances in consciousness NEC(MedDRA:10013509) Syncope(HPO:0001279) |
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Database Frequency: | 94 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
AL amyloidosis | (Orphanet:85443) |
Arrhythmogenic right ventricular dysplasia, familial, 10 | (OMIM:610193) |
Arrhythmogenic right ventricular dysplasia, familial, 11 | (OMIM:610476) |
Arrhythmogenic right ventricular dysplasia, familial, 12 | (OMIM:611528) |
Arrhythmogenic right ventricular dysplasia, familial, 13 | (OMIM:615616) |
Arrhythmogenic right ventricular dysplasia, familial, 3 | (OMIM:602086) |
Arrhythmogenic right ventricular dysplasia, familial, 4 | (OMIM:602087) |
Arrhythmogenic right ventricular dysplasia, familial, 5 | (OMIM:604400) |
Arrhythmogenic right ventricular dysplasia, familial, 6 | (OMIM:604401) |
Arrhythmogenic right ventricular dysplasia, familial, 9 | (OMIM:609040) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Atrial fibrillation, familial, 17 | (ORPHA:334) |
Atrial fibrillation, familial, 3 | (OMIM:607554) |
Atrial standstill | (Orphanet:1344) |
Atrial standstill 1 | (OMIM:108770) |
Atrial standstill 2 | (OMIM:615745) |
BRUGADA SYNDROME 2 | (OMIM:611777) |
BRUGADA SYNDROME 3 | (OMIM:611875) |
BRUGADA SYNDROME 4 | (OMIM:611876) |
Brugada syndrome | (Orphanet:130) |
CARDIAC CONDUCTION DEFECTSUDDEN CARDIAC DEATH, INCLUDED | (OMIM:115080) |
Cardiac arrhythmia, ankyrin-B-related | (OMIM:600919) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cardiomyopathy, dilated, 1E | (OMIM:601154) |
Cardiomyopathy, dilated, 1R | (OMIM:613424) |
Cardiomyopathy, dilated, 1U | (OMIM:613694) |
Cardiomyopathy, dilated, 1V | (OMIM:613697) |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | (OMIM:615821) |
Cardiomyopathy, familial hypertrophic, 1 | (OMIM:192600) |
Cardiomyopathy, familial hypertrophic, 13 | (OMIM:613243) |
Cardiomyopathy, familial hypertrophic, 14 | (OMIM:613251) |
Cardiomyopathy, familial hypertrophic, 16 | (OMIM:613838) |
Cardiomyopathy, familial hypertrophic, 2 | (OMIM:115195) |
Cardiomyopathy, familial hypertrophic, 4 | (OMIM:115197) |
Cardiomyopathy, familial restrictive, 1 | (OMIM:115210) |
Catecholaminergic polymorphic ventricular tachycardia | (Orphanet:3286) |
Fabry disease | (Orphanet:324) |
Familial atrial fibrillation | (Orphanet:334) |
Familial atrial myxoma | (Orphanet:615) |
Familial isolated arrhythmogenic right ventricular dysplasia | (Orphanet:217656) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Familial long QT syndrome | (Orphanet:768) |
Familial progressive cardiac conduction defect | (Orphanet:871) |
Familial short QT syndrome | (Orphanet:51083) |
Familial sick sinus syndrome | (Orphanet:166282) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Glycogen storage disease due to muscle and heart glycogen synthase deficiency | (Orphanet:137625) |
Hereditary sensory and autonomic neuropathy type 1B | (Orphanet:139564) |
Idiopathic giant cell myocarditis | (Orphanet:329874) |
Idiopathic ventricular fibrillation, not Brugada type | (Orphanet:228140) |
Incessant infant ventricular tachycardia | (Orphanet:45453) |
Jervell and Lange-Nielsen syndrome | (Orphanet:90647) |
Jervell and Lange-Nielsen syndrome 1 | (OMIM:220400) |
Jervell and Lange-Nielsen syndrome 2 | (OMIM:612347) |
Left ventricular noncompaction | (Orphanet:54260) |
Left ventricular noncompaction 10 | (OMIM:615396) |
Long QT syndrome 1 | (OMIM:192500) |
Long QT syndrome 12 | (OMIM:612955) |
Long QT syndrome 13 | (OMIM:613485) |
Long QT syndrome 2 | (OMIM:613688) |
Long QT syndrome 3 | (OMIM:603830) |
Long QT syndrome 5 | (OMIM:613695) |
Long QT syndrome 6 | (OMIM:613693) |
Naxos disease | (Orphanet:34217) |
ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE | (OMIM:143850) |
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB | (OMIM:604559) |
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II | (OMIM:140400) |
PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:265400) |
Papillary fibroelastoma of the heart | (Orphanet:208600) |
Peripartum cardiomyopathy | (Orphanet:563) |
Primary systemic amyloidosis | (Orphanet:314701) |
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome | (Orphanet:228012) |
Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
Pulmonary venoocclusive disease | (Orphanet:31837) |
Romano-Ward syndrome | (Orphanet:101016) |
SHORT QT SYNDROME 2 | (OMIM:609621) |
Sarcoidosis | (Orphanet:797) |
Senile systemic amyloidosis | (Orphanet:330001) |
Sino-auricular heart block | (Orphanet:1260) |
Sinoatrial node dysfunction and deafness | (Orphanet:324321) |
TENORIO SYNDROME | (OMIM:616260) |
Tako-Tsubo cardiomyopathy | (Orphanet:66529) |
Timothy syndrome | (Orphanet:65283) |
Torsade-de-pointes syndrome with short coupling interval | (Orphanet:51084) |
Uhl anomaly | (Orphanet:3403) |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH ORWITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY | (OMIM:604772) |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2 | (OMIM:611938) |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3 | (OMIM:614021) |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4 | (OMIM:614916) |
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence | (Orphanet:3201) |
Wilson disease | (Orphanet:905) |
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 | (OMIM:107970) |