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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: Calcinosis (D002114)
Parent Node: Coronary Artery Disease (D003324)
..Starting node ..Coronary Sclerosis, Medial, of Infancy (C565944)
Child Nodes:
Sister Nodes:
..Coronary Artery Disease, Autosomal Dominant 2 (C567045)
..Coronary Artery Disease, Autosomal Dominant, 1 (C564258)
..Coronary Artery Disease, Development of, in HIV (C563569)
..Coronary Sclerosis, Medial, of Infancy (C565944)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	2763
Name:	Coronary Sclerosis, Medial, of Infancy
Definition:
Alternative IDs:
ParentIDs:	MESH:D002114\|MESH:D003324
TreeNumbers:	C14.280.647.250.260/C565944 \|C14.907.137.126.339/C565944 \|C14.907.585.250.260/C565944 \|C18.452.174.130/C565944
Synonyms:
Slim Mappings:	Cardiovascular disease\|Metabolic disease
Reference:	MedGen: C565944 MeSH: C565944 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants