coronary artery disease Disease Ontology Browser

Disease Ontology Browser

coronary artery disease (DOID:3393)
Alliance: disease page
Synonyms: CHD; coronary arteriosclerosis; Coronary disease; coronary heart disease
Alt IDs: OMIM:300464, OMIM:607339, OMIM:608316, OMIM:608318, OMIM:608320, OMIM:610947, OMIM:611139, OMIM:612030, OMIM:614293, DOID:10506, DOID:3363, DOID:3394, DOID:9420, EFO:0001645, ICD10CM:I20-I25, ICD10CM:I25, ICD10CM:I25.10, ICD9CM:410-414.99, ICD9CM:414.0, ICD9CM:414.9, MESH:D003324, MESH:D003327, MESH:D017202, NCI:C35505, NCI:C50625, UMLS_CUI:C0010054, UMLS_CUI:C0010068, UMLS_CUI:C0151744, UMLS_CUI:C0264694
Definition: An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.

Disease References using Mouse Models (3)

Allelic Composition	Genetic Background	Reference	Phenotypes
Kcnj8tm1Sse/Kcnj8tm1Sse	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	J:76195	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Abcc9tm1Cfb/Abcc9tm1Cfb	Not Specified	J:78066	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Apoetm1Unc/Apoetm1Unc Scarb1tm1Kri/Scarb1tm1Kri	involves: 129P2/OlaHsd * 129S2/SvPas * BALB/c * C57BL/6	J:201999	View

Allelic Composition	Genetic Background	Reference	Phenotypes
Apoetm1Unc/Apoetm1Unc Svep1em1Nost/Svep1em1Nost	involves: 129P2/OlaHsd * C57BL/6	J:304349	View

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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