Cardiac arrest

Symptom Information:

Symptom ID: HPO:0001695
Synonyms:
Asystole (disorder) [Orphanet:35120]
Cardiorespiratory arrest (disorder) [Orphanet:35120]
Cardiac arrest (disorder) [Orphanet:35120]
Cardiopulmonary Arrest [Orphanet:35120]
Cardiac Arrest [Orphanet:35120]
Cardiac arrest [OMIM:Cardiac arrest]
Collapse/sudden death/cardiac arrest/cardiorespiratory arrest [Orphanet:35120]
Cardio-respiratory arrest [Orphanet:35120]
Ventricular asystole [Orphanet:35120]
Cardio-respiratory arrest [MedDRA:10007617]
Cardiopulmonary arrest [MedDRA:10007617]
Ventricular asystole [MedDRA:10047284]
Ventricular asystolia [MedDRA:10047284]
Cardiac arrest [MedDRA:10007515]
Quality:
Cross references:
HPO:0006543 "Cardiorespiratory arrest" [Orphanet:35120]
Orphanet:35120 "Collapse/sudden death/cardiac arrest/cardiorespiratory arrest" [Orphanet:35120]
OMIM: "Cardiac arrest" [OMIM:Cardiac arrest]
UMLS:C0600228 "Cardiopulmonary Arrest" [Orphanet:35120]
UMLS:C0018790 "Cardiac Arrest" [Orphanet:35120]
Is a (Direct Parents):
Orphanet Abnormality of cardiovascular system physiology
HPO         Arrhythmia
MedDRA Ventricular arrhythmias and cardiac arrest
Orphanet Congestive heart failure
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)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
                Cardiac arrest(HPO:0001695)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
                Cardiac arrest(HPO:0001695)
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)