Sudden cardiac death

Symptom Information:

Symptom ID: HPO:0001645
Synonyms:
Premature sudden cardiac death [HPO:0001645]
Sudden death [Orphanet:35120]
Sudden cardiac death (disorder) [Orphanet:35120]
Sudden death (event) [Orphanet:35120]
Sudden Cardiac Death [Orphanet:35120]
Premature sudden cardiac death [OMIM:Premature sudden cardiac death]
Sudden cardiac death [OMIM:Sudden cardiac death]
Collapse/sudden death/cardiac arrest/cardiorespiratory arrest [Orphanet:35120]
Sudden cardiac death [Orphanet:35120]
Sudden cardiac death [MedDRA:10049418]
Sudden arrhythmic death syndrome [MedDRA:10049418]
Sudden death [MedDRA:10042434]
Death occurring in less than 24 hours from onset of symptoms, not otherwise explained [MedDRA:10042434]
Death sudden (NOS) [MedDRA:10042434]
Instantaneous death [MedDRA:10042434]
Sudden death NOS [MedDRA:10042434]
Sudden death unexplained [MedDRA:10042434]
Sudden death, cause unknown [MedDRA:10042434]
Death sudden [MedDRA:10042434]
Sudden cardiac death (in some patients) [OMIM:Sudden cardiac death (in some patients)]
Sudden death (rare) [OMIM:Sudden death (rare)]
Quality:
Cross references:
HPO:0001699 "Sudden death" [Orphanet:35120]
Orphanet:35120 "Collapse/sudden death/cardiac arrest/cardiorespiratory arrest" [Orphanet:35120]
OMIM: "Premature sudden cardiac death" [OMIM:Premature sudden cardiac death]
OMIM: "Sudden cardiac death" [OMIM:Sudden cardiac death]
OMIM: "Sudden cardiac death (in some patients)" [OMIM:Sudden cardiac death (in some patients)]
OMIM: "Sudden death (rare)" [OMIM:Sudden death (rare)]
UMLS:C0011071 "Sudden death" [Orphanet:35120]
UMLS:C0085298 "Sudden Cardiac Death" [Orphanet:35120]
Is a (Direct Parents):
HPO         Cardiac arrest
MedDRA Ventricular arrhythmias and cardiac arrest
Orphanet Congestive heart failure
Orphanet Abnormality of cardiovascular system physiology
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)
             Arrhythmia(HPO:0011675)
                Cardiac arrest(HPO:0001695)
                   Sudden cardiac death(HPO:0001645)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Arrhythmia(HPO:0011675)
       Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
          Sudden cardiac death(HPO:0001645)
Investigations(MedDRA:10022891)
    Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
                Sudden cardiac death(HPO:0001645)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
                Sudden cardiac death(HPO:0001645)
Database Frequency: 84 / 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, 2 (OMIM:600996)
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, 8 (OMIM:607450)
Arrhythmogenic right ventricular dysplasia, familial, 9 (OMIM:609040)
Atrial fibrillation, familial, 9 (OMIM:613980)
Atrial standstill (Orphanet:1344)
Autosomal dominant limb-girdle muscular dystrophy type 1B (Orphanet:264)
BRUGADA SYNDROME 2 (OMIM:611777)
BRUGADA SYNDROME 3 (OMIM:611875)
Barth syndrome (Orphanet:111)
Becker muscular dystrophy (Orphanet:98895)
Brugada syndrome (Orphanet:130)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 (OMIM:617047)
Cardiac arrhythmia, ankyrin-B-related (OMIM:600919)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cardiomyopathy, dilated, 1C (OMIM:601493)
Cardiomyopathy, dilated, 1D (OMIM:601494)
Cardiomyopathy, dilated, 1DD (OMIM:613172)
Cardiomyopathy, dilated, 1L (OMIM:606685)
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis (OMIM:615821)
Cardiomyopathy, familial hypertrophic, 1 (OMIM:192600)
Cardiomyopathy, familial hypertrophic, 12 (OMIM:612124)
Cardiomyopathy, familial hypertrophic, 21 (OMIM:614676)
Cardiomyopathy, familial hypertrophic, 3 (OMIM:115196)
Cardiomyopathy, familial hypertrophic, 4 (OMIM:115197)
Cardiomyopathy, familial hypertrophic, 6 (OMIM:600858)
Cardiomyopathy, familial hypertrophic, 7 (OMIM:613690)
Cardiomyopathy, familial hypertrophic, 8 (OMIM:608751)
Cardiomyopathy, familial hypertrophic, 9 (OMIM:613765)
Carney complex (Orphanet:1359)
Catecholaminergic polymorphic ventricular tachycardia (Orphanet:3286)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
Desminopathy (Orphanet:98909)
Dilated cardiomyopathy with ataxia (Orphanet:66634)
Duchenne muscular dystrophy (Orphanet:98896)
Ebstein malformation (Orphanet:1880)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
Fabry disease (Orphanet:324)
Familial atrial fibrillation (Orphanet:334)
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation (Orphanet:300751)
Familial isolated hypertrophic cardiomyopathy (Orphanet:155)
Familial long QT syndrome (Orphanet:768)
Familial progressive cardiac conduction defect (Orphanet:871)
Familial short QT syndrome (Orphanet:51083)
His bundle tachycardia (Orphanet:3283)
Histiocytoid cardiomyopathy (Orphanet:137675)
Hypertrophic cardiomyopathy due to intensive athletic training (Orphanet:217601)
Idiopathic giant cell myocarditis (Orphanet:329874)
Idiopathic neonatal atrial flutter (Orphanet:45452)
Idiopathic ventricular fibrillation, not Brugada type (Orphanet:228140)
Jervell and Lange-Nielsen syndrome (Orphanet:90647)
Jervell and Lange-Nielsen syndrome 1 (OMIM:220400)
Left ventricular noncompaction 1 (OMIM:604169)
Left ventricular noncompaction 2 (OMIM:609470)
Long QT syndrome 1 (OMIM:192500)
Long QT syndrome 10 (OMIM:611819)
Long QT syndrome 2 (OMIM:613688)
Long QT syndrome 3 (OMIM:603830)
Long QT syndrome 5 (OMIM:613695)
Long QT syndrome 6 (OMIM:613693)
MELAS (Orphanet:550)
Naxos disease (Orphanet:34217)
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II (OMIM:140400)
Peripartum cardiomyopathy (Orphanet:563)
Romano-Ward syndrome (Orphanet:101016)
SHORT QT SYNDROME 2 (OMIM:609621)
Sarcoidosis (Orphanet:797)
Sensorineural deafness with dilated cardiomyopathy (Orphanet:217622)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Timothy syndrome (Orphanet:65283)
Torsade-de-pointes syndrome with short coupling interval (Orphanet:51084)
Uhl anomaly (Orphanet:3403)
VENTRICULAR TACHYCARDIA, FAMILIAL (OMIM:192605)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)
WOLFF-PARKINSON-WHITE SYNDROME (OMIM:194200)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 (OMIM:107970)
[DEL]EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED (OMIM:310300)