Syncope

Symptom Information:

Symptom ID: HPO:0001279
Synonyms:
Syncope [OMIM:Syncope]
Syncope [MedDRA:10042772]
Quality:
Cross references:
OMIM: "Syncope" [OMIM:Syncope]
UMLS:C0039070 "Syncope" [HPO:0001279]
Is a (Direct Parents):
HPO         Abnormality of cardiovascular system physiology
MedDRA Disturbances in consciousness NEC
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)
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)