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: Angina Pectoris (D000787)
Parent Node: Myocardial Ischemia (D017202)
..Starting node ..Acute Coronary Syndrome (D054058)
Child Nodes:
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:	234
Name:	Acute Coronary Syndrome
Definition:	An episode of MYOCARDIAL ISCHEMIA that generally lasts longer than a transient anginal episode that ultimately may lead to MYOCARDIAL INFARCTION.
Alternative IDs:
ParentIDs:	MESH:D000787\|MESH:D017202
TreeNumbers:	C14.280.647.124 \|C14.280.647.187.074 \|C14.907.585.124 \|C14.907.585.187.074 \|C23.888.646.215.500.074
Synonyms:	Acute Coronary Syndromes \|Coronary Syndrome, Acute \|Coronary Syndromes, Acute \|Syndrome, Acute Coronary \|Syndromes, Acute Coronary
Slim Mappings:	Cardiovascular disease\|Signs and symptoms
Reference:	MedGen: D054058 MeSH: D054058 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants