Disease browser and phenotype portal

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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: Chest Pain (D002637)
Parent Node: Myocardial Ischemia (D017202)
..Starting node ..Angina Pectoris (D000787)
Child Nodes:
........Acute Coronary Syndrome (D054058)
........Angina, Stable (D060050)
........Angina, Unstable (D000789) 2
........Microvascular Angina (D017566)
Sister Nodes:
..Acute Coronary Syndrome (D054058)
..Angina Pectoris (D000787) 6
..Coronary Disease (D003327) 13
..Myocardial Infarction (D009203) 7
..Myocardial Reperfusion Injury (D015428)
..Myocardial Stunning (D017682)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	676
Name:	Angina Pectoris
Definition:	The symptom of paroxysmal pain consequent to MYOCARDIAL ISCHEMIA usually of distinctive character, location and radiation. It is thought to be provoked by a transient stressful situation during which the oxygen requirements of the MYOCARDIUM exceed that supplied by the CORONARY CIRCULATION.
Alternative IDs:
ParentIDs:	MESH:D002637\|MESH:D017202
TreeNumbers:	C14.280.647.187 \|C14.907.585.187 \|C23.888.646.215.500
Synonyms:	Angor Pectoris \|Stenocardia \|Stenocardias
Slim Mappings:	Cardiovascular disease\|Signs and symptoms
Reference:	MedGen: D000787 MeSH: D000787 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants