loading...| Preferred Name |
Atrial Fibrillation |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C50466 |
| ALT_DEFINITION |
Irregular heart rhythm, usually associated with a rapid rate, that is caused by abnormal electrical activity within the atrial. An irregular heart rhythm, usually associated with a rapid rate, that is caused by abnormal electrical activity within the atria. A disorder characterized by a dysrhythmia without discernible P waves and an irregular ventricular response due to multiple reentry circuits. The rhythm disturbance originates above the ventricles. |
| code |
C50466 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C158520 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C177537 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C157711 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C189762 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118464 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C62596 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C156952 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C158035 |
| Contributing_Source |
MedDRA CPTAC NICHD GDC FDA Cellosaurus CTCAE |
| DEFINITION |
A disorder characterized by an electrocardiographic finding of a supraventricular arrhythmia characterized by the replacement of consistent P waves by rapid oscillations or fibrillatory waves that vary in size, shape and timing and are accompanied by an irregular ventricular response. (CDISC) |
| FDA_Table |
Patient Code (Appendix B) |
| FULL_SYN |
Atrial fibrillation Atrial Fibrillation AF AFib |
| Is_Value_For_GDC_Property | |
| label |
Atrial Fibrillation |
| Legacy Concept Name |
Atrial_Fibrillation |
| Maps_To |
Atrial fibrillation Atrial Fibrillation |
| Preferred_Name |
Atrial Fibrillation |
| prefixIRI |
Thesaurus:C50466 |
| prefLabel |
Atrial Fibrillation |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C4015486 |
| xRef |
IMDRF:E060102 |
| subClassOf |