Sudden death
Symptom Information:
Symptom ID: | HPO:0001699 | ||||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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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) ECG investigations(MedDRA:10053104) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Sudden death(HPO:0001699) Heart rate and pulse investigations(MedDRA:10053103) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Sudden death(HPO:0001699) |
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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) |