Disease Browser
Parent Node: Arrhythmias, Cardiac (D001145) ..Starting node .. Commotio Cordis (D056104) Child Nodes:
Sister Nodes: ..Arrhythmia, Sinus (D001146) 5 ..Atrial Fibrillation (D001281) 8 ..Atrial Flutter (D001282) ..Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects (C566351) ..Bradycardia (D001919) ..Brugada Syndrome (D053840) 9 ..Cardiac Arrhythmia, Ankyrin-B-Related (C566996) ..Cardiac Complexes, Premature (D005117) 4 ..Cardiac Conduction Defect (C562490) ..Cardiac Conduction Defect, Nonprogressive (C566186) ..Commotio Cordis (D056104) ..Heart Block (D006327) 19 ..Long QT Syndrome (D008133) 20 ..Parasystole (D017574) ..Pre-Excitation Syndromes (D011226) 3 ..QT INTERVAL, VARIATION IN (OMIM:610141) ..Short Qt Syndrome (C580439) ..Short QT Syndrome 1 (C566506) ..Short QT Syndrome 2 (C566505) ..Short QT Syndrome 3 (C566504) ..Simpson-Golabi-Behmel syndrome (C537340) ..Tachycardia (D013610) 20 ..Ventricular Fibrillation (D014693) 3 ..Ventricular Flutter (D054141) ..Woodhouse Sakati syndrome (C536742) Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 2541
Name: Commotio Cordis
Definition: A sudden CARDIAC ARRHYTHMIA (e.g., VENTRICULAR FIBRILLATION) caused by a blunt, non-penetrating impact to the precordial region of chest wall. Commotio cordis often results in sudden death without prompt cardiopulmonary defibrillation.
Alternative IDs:
ParentIDs: MESH:D001145
TreeNumbers: C14.280.067.441
Synonyms: Cardiac Concussion |Cardiac Concussions |Concussion, Cardiac |Concussions, Cardiac
Slim Mappings: Cardiovascular disease
Reference:
MedGen: D056104
MeSH: D056104
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants