Cardiac arrest
Symptom Information:
Symptom ID: | HPO:0001695 | ||||||||||||||
Synonyms: |
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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) Arrhythmia(HPO:0011675) Cardiac arrest(HPO:0001695) MedDRA: Cardiac disorders(MedDRA:10007541) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Cardiac arrest(HPO:0001695) 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) Cardiac arrest(HPO:0001695) ECG investigations(MedDRA:10053104) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Cardiac arrest(HPO:0001695) |
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Database Frequency: | 87 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
Achondroplasia | (Orphanet:15) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alexander disease | (Orphanet:58) |
Anisakiasis | (Orphanet:1070) |
Arrhythmogenic right ventricular dysplasia, familial, 11 | (OMIM:610476) |
Arrhythmogenic right ventricular dysplasia, familial, 9 | (OMIM:609040) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Atrial fibrillation, familial, 3 | (OMIM:607554) |
Atrial standstill | (Orphanet:1344) |
BRUGADA SYNDROME 1 | (OMIM:601144) |
BRUGADA SYNDROME 6 | (OMIM:613119) |
Beta-thalassemia major | (Orphanet:231214) |
Bullous diffuse cutaneous mastocytosis | (Orphanet:280785) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction | (OMIM:612158) |
Carney complex | (Orphanet:1359) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Carnitine palmitoyl transferase II deficiency | (Orphanet:157) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Catecholaminergic polymorphic ventricular tachycardia | (Orphanet:3286) |
Cholera | (Orphanet:173) |
Combined oxidative phosphorylation defect type 9 | (Orphanet:319509) |
Crimean-Congo hemorrhagic fever | (Orphanet:99827) |
Cutaneous mastocytosis | (Orphanet:66646) |
Dengue fever | (Orphanet:99828) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
Ebola hemorrhagic fever | (Orphanet:319218) |
Ebstein malformation | (Orphanet:1880) |
Familial isolated arrhythmogenic right ventricular dysplasia | (Orphanet:217656) |
Familial long QT syndrome | (Orphanet:768) |
Familial short QT syndrome | (Orphanet:51083) |
Febrile infection-related epilepsy syndrome | (Orphanet:163703) |
Foodborne botulism | (Orphanet:228371) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Giant cell arteritis | (Orphanet:397) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
Harlequin ichthyosis | (Orphanet:457) |
Histiocytoid cardiomyopathy | (Orphanet:137675) |
Hughes-Stovin syndrome | (Orphanet:228116) |
Hypoalphalipoproteinemia | (Orphanet:31153) |
Indolent systemic mastocytosis | (Orphanet:98848) |
Infant botulism | (Orphanet:178478) |
Jervell and Lange-Nielsen syndrome | (Orphanet:90647) |
Lassa fever | (Orphanet:99824) |
Leprechaunism | (Orphanet:508) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
Long QT syndrome 1 | (OMIM:192500) |
Long QT syndrome 2 | (OMIM:613688) |
Long QT syndrome 3 | (OMIM:603830) |
Lujo hemorrhagic fever | (Orphanet:319213) |
Lyell syndrome | (Orphanet:537) |
MELAS | (Orphanet:550) |
Maculopapular cutaneous mastocytosis | (Orphanet:79457) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Narcolepsy-cataplexy | (Orphanet:2073) |
Naxos disease | (Orphanet:34217) |
PAGOD syndrome | (Orphanet:991) |
PGM1-CDG | (Orphanet:319646) |
Polyvalvular heart disease syndrome | (Orphanet:228410) |
Porphyria cutanea tarda | (Orphanet:101330) |
Proteus syndrome | (Orphanet:744) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Pulmonary arterial hypertension | (Orphanet:182090) |
Pyomyositis | (Orphanet:764) |
Rabies | (Orphanet:770) |
Rift valley fever | (Orphanet:319251) |
Romano-Ward syndrome | (Orphanet:101016) |
Sino-auricular heart block | (Orphanet:1260) |
Sinus node disease and myopia | (OMIM:182190) |
Spondylometaphyseal dysplasia, Sedaghatian type | (Orphanet:93317) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Systemic capillary leak syndrome | (Orphanet:188) |
Systemic mastocytosis | (Orphanet:2467) |
Tako-Tsubo cardiomyopathy | (Orphanet:66529) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Thymic tumor | (Orphanet:100100) |
Torsade-de-pointes syndrome with short coupling interval | (Orphanet:51084) |
Typhoid | (Orphanet:99745) |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4 | (OMIM:614916) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |
Williams syndrome | (Orphanet:904) |
Wiskott-Aldrich syndrome | (Orphanet:906) |
Wound botulism | (Orphanet:178475) |
Yellow fever | (Orphanet:99829) |