Cardiorespiratory arrest
Symptom Information:
Symptom ID: | HPO:0006543 | ||||||||||||||||
Synonyms: |
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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 respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Respiratory insufficiency(HPO:0002093) Respiratory arrest(HPO:0005943) Cardiorespiratory arrest(HPO:0006543) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Respiratory insufficiency(HPO:0002093) Respiratory arrest(HPO:0005943) Cardiorespiratory arrest(HPO:0006543) MedDRA: Cardiac disorders(MedDRA:10007541) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Cardiorespiratory arrest(HPO:0006543) 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) Cardiorespiratory arrest(HPO:0006543) Heart rate and pulse investigations(MedDRA:10053103) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Cardiorespiratory arrest(HPO:0006543) |
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Database Frequency: | 11 / 7739 | ||||||||||||||||
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All diseases associated with this symptom:
Brugada syndrome | (Orphanet:130) |
Carney complex | (Orphanet:1359) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
Fetal Gaucher disease | (Orphanet:85212) |
MELAS | (Orphanet:550) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |