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: Myocardial Infarction (D009203)
Parent Node: Shock (D012769)
..Starting node ..Shock, Cardiogenic (D012770)
Child Nodes:
Sister Nodes:
..Multiple Organ Failure (D009102)
..Shock, Cardiogenic (D012770)
..Shock, Hemorrhagic (D012771)
..Shock, Surgical (D012773)
..Shock, Traumatic (D012774) 1
..Systemic Inflammatory Response Syndrome (D018746) 11
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10180
Name:	Shock, Cardiogenic
Definition:	Shock resulting from diminution of cardiac output in heart disease.
Alternative IDs:
ParentIDs:	MESH:D009203\|MESH:D012769
TreeNumbers:	C14.280.647.500.750 \|C14.907.585.500.750 \|C23.550.835.550
Synonyms:	Cardiogenic Shock
Slim Mappings:	Cardiovascular disease\|Pathology (process)
Reference:	MedGen: D012770 MeSH: D012770 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants