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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: Arteriosclerosis (D001161)
..Starting node ..Atherosclerosis (D050197)
Child Nodes:
........Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease (C565928)
........Carotid Intimal Medial Thickness 1 (C563733)
........Peripheral Arterial Disease (D058729) 2
Sister Nodes:
..Arteriolosclerosis (D050379)
..Arteriosclerosis Obliterans (D001162)
..Arteriosclerosis, Severe Juvenile (C565941)
..Atherosclerosis (D050197) 5
..Coronary Artery Disease (D003324) 4
..Feigenbaum Bergeron Richardson syndrome (C536178)
..Intermittent Claudication (D007383)
..Intracranial Arteriosclerosis (D002537) 4
..Schimke immunoosseous dysplasia (C536629)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

1003

Name:

Atherosclerosis

Definition:

A thickening and loss of elasticity of the walls of ARTERIES that occurs with formation of ATHEROSCLEROTIC PLAQUES within the ARTERIAL INTIMA.

Alternative IDs:

OMIM:108725

ParentIDs:

MESH:D001161

TreeNumbers:

C14.907.137.126.307

Synonyms:

Slim Mappings:

Cardiovascular disease

Reference:

MedGen: D050197
MeSH: D050197
OMIM: 108725;

Genes: ATHS;

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0003233	Decreased HDL cholesterol concentration
3	HP:0002155	Hypertriglyceridemia
4	HP:0001658	Myocardial infarction

Disease Causing ClinVar Variants