Sudden death

Symptom Information:

Symptom ID: HPO:0001699
Synonyms:
Sudden cardiac death (disorder) [Orphanet:35120]
Sudden death (event) [Orphanet:35120]
Sudden death [Orphanet:35120]
Sudden Cardiac Death [Orphanet:35120]
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:0001645 "Sudden cardiac death" [Orphanet:35120]
Orphanet:35120 "Collapse/sudden death/cardiac arrest/cardiorespiratory arrest" [Orphanet:35120]
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):
Orphanet Congestive heart failure
HPO         Death
MedDRA Ventricular arrhythmias and cardiac arrest
Orphanet Abnormality of cardiovascular system physiology
Is a (Whole tree): HPO:
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Arrhythmia(HPO:0011675)
       Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
          Sudden death(HPO:0001699)
Investigations(MedDRA:10022891)
    Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
                Sudden death(HPO:0001699)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
                Sudden death(HPO:0001699)
Database Frequency: 34 / 7739
Resource:

All diseases associated with this symptom:

APNEA, CENTRAL SLEEP (OMIM:107640)
Arrhythmogenic right ventricular dysplasia, familial, 2 (OMIM:600996)
CARDIAC ARRHYTHMIA (OMIM:115000)
CARDIAC CONDUCTION DEFECTSUDDEN CARDIAC DEATH, INCLUDED (OMIM:115080)
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction (OMIM:612158)
Cardiomyopathy, dilated, 1EE (OMIM:613252)
Cardiomyopathy, dilated, 1KK (OMIM:615248)
Cardiomyopathy, dilated, 1S (OMIM:613426)
Cardiomyopathy, dilated, 1W (OMIM:611407)
Cardiomyopathy, dilated, 1Z (OMIM:611879)
Cardiomyopathy, familial hypertrophic, 2 (OMIM:115195)
Cardiomyopathy, familial restrictive, 1 (OMIM:115210)
Cardiomyopathy, hypertrophic, 25 (OMIM:607487)
Catecholaminergic polymorphic ventricular tachycardia (Orphanet:3286)
Costello syndrome (Orphanet:3071)
Early-onset myopathy with fatal cardiomyopathy (Orphanet:289377)
Familial atrial myxoma (Orphanet:615)
Familial isolated arrhythmogenic right ventricular dysplasia (Orphanet:217656)
Familial isolated dilated cardiomyopathy (Orphanet:154)
Familial isolated restrictive cardiomyopathy (Orphanet:75249)
Familial progressive cardiac conduction defect (Orphanet:871)
Heart-hand syndrome, Slovenian type (Orphanet:168796)
Left ventricular noncompaction (Orphanet:54260)
Leprechaunism (Orphanet:508)
Naxos disease (Orphanet:34217)
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II (OMIM:140400)
Papillary fibroelastoma of the heart (Orphanet:208600)
SUDDEN INFANT DEATH SYNDROME (OMIM:272120)
Sclerosteosis (Orphanet:3152)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2 (OMIM:611938)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3 (OMIM:614021)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4 (OMIM:614916)
Williams syndrome (Orphanet:904)
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome (Orphanet:65282)