Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Cardiomyopathies (D009202)
Parent Node: Myocardial Ischemia (D017202)
Parent Node: Reperfusion Injury (D015427)
..Starting node ..Myocardial Reperfusion Injury (D015428)
Child Nodes:
Sister Nodes:
..Myocardial Reperfusion Injury (D015428)
..Primary Graft Dysfunction (D055031)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7632
Name:	Myocardial Reperfusion Injury
Definition:	Damage to the MYOCARDIUM resulting from MYOCARDIAL REPERFUSION (restoration of blood flow to ischemic areas of the HEART.) Reperfusion takes place when there is spontaneous thrombolysis, THROMBOLYTIC THERAPY, collateral flow from other coronary vascular beds, or reversal of vasospasm.
Alternative IDs:
ParentIDs:	MESH:D009202\|MESH:D015427\|MESH:D017202
TreeNumbers:	C14.280.238.615 \|C14.280.647.625 \|C14.907.585.625 \|C14.907.725.600 \|C23.550.767.877.500
Synonyms:	Injuries, Myocardial Reperfusion \|Injury, Myocardial Reperfusion \|Myocardial Ischemic Reperfusion Injury \|Myocardial Reperfusion Injuries \|Reperfusion Injuries, Myocardial \|Reperfusion Injury, Myocardial
Slim Mappings:	Cardiovascular disease\|Pathology (process)
Reference:	MedGen: D015428 MeSH: D015428 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants