Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandMyocardial Infarction (D009203)
Parent Node:
expandMyocardial Ischemia (D017202)
..Starting node
..expandMyocardial Stunning (D017682)

       Child Nodes:



 Sister Nodes: 
..expandAcute Coronary Syndrome (D054058)
..expandAngina Pectoris (D000787) Child6
..expandCoronary Disease (D003327) Child13
..expandMyocardial Infarction (D009203) Child7
..expandMyocardial Reperfusion Injury (D015428)
..expandMyocardial Stunning (D017682)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:7633
Name:Myocardial Stunning
Definition:Prolonged dysfunction of the myocardium after a brief episode of severe ischemia, with gradual return of contractile activity. It occurs frequently, both in the experimental laboratory and in clinical medicine. Since stunned myocardium occurs adjacent to necrotic tissue after prolonged coronary occlusion, many myocardial infarcts may be a mixture of necrotic and stunned tissue. (Braunwald, Heart Disease, 1992, p1176)
Alternative IDs:
ParentIDs:MESH:D009203|MESH:D017202
TreeNumbers:C14.280.647.500.375 |C14.280.647.750 |C14.907.585.500.375 |C14.907.585.750
Synonyms:Hibernation, Myocardial |Myocardial Hibernation |Myocardium, Stunned |Stunned Myocardium |Stunning, Myocardial
Slim Mappings:Cardiovascular disease
Reference: MedGen: D017682
MeSH: D017682
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants