Coronary artery disease

Symptom Information:

Symptom ID: HPO:0001677
Synonyms:
Coronary disease [HPO:0001677]
Coronary artery disease [OMIM:Coronary artery disease]
Coronary artery disease (in some patients) [OMIM:Coronary artery disease (in some patients)]
Coronary artery disease [MedDRA:10011078]
Quality:
Cross references:
OMIM: "Coronary artery disease" [OMIM:Coronary artery disease]
OMIM: "Coronary artery disease (in some patients)" [OMIM:Coronary artery disease (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the coronary arteries
MedDRA Coronary necrosis and vascular insufficiency
HPO         Atherosclerosis
HPO         Arterial stenosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Arteriosclerosis(HPO:0002634)
                Atherosclerosis(HPO:0002621)
                   Coronary artery disease(HPO:0001677)
             Abnormality of the systemic arterial tree(HPO:0011004)
                Abnormality of the coronary arteries(HPO:0006704)
                   Coronary artery disease(HPO:0001677)
                Abnormalities of the peripheral arteries(HPO:0005114)
                   Arterial stenosis(HPO:0100545)
                      Coronary artery disease(HPO:0001677)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216)
       Coronary necrosis and vascular insufficiency(MedDRA:10065875)
          Coronary artery disease(HPO:0001677)
Database Frequency: 58 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
AORTIC ANEURYSM, FAMILIAL THORACIC 4 (OMIM:132900)
Alkaptonuria (Orphanet:56)
Arterial tortuosity syndrome (Orphanet:3342)
Babesiosis (Orphanet:108)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Bardet-Biedl syndrome 2 (OMIM:615981)
Behçet disease (Orphanet:117)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 (OMIM:608320)
Cardiomyopathy, dilated, 1S (OMIM:613426)
Cerebrotendinous xanthomatosis (Orphanet:909)
Chronic hiccup (Orphanet:396)
Cogan syndrome (Orphanet:1467)
Combined pulmonary fibrosis-emphysema syndrome (Orphanet:300564)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
Cutaneous mastocytosis (Orphanet:66646)
Dermatomyositis (Orphanet:221)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Essential thrombocythemia (Orphanet:3318)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Familial cutaneous collagenoma (Orphanet:53296)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy due to AKT2 mutations (Orphanet:79085)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Familial partial lipodystrophy, Köbberling type (Orphanet:79084)
Fish-eye disease (Orphanet:79292)
Gastrocutaneous syndrome (Orphanet:2069)
Giant cell arteritis (Orphanet:397)
Granulomatosis with polyangiitis (Orphanet:900)
HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B (OMIM:144010)
Hurler syndrome (Orphanet:93473)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hypoalphalipoproteinemia (Orphanet:31153)
Juvenile dermatomyositis (Orphanet:93672)
Kawasaki disease (Orphanet:2331)
Lyell syndrome (Orphanet:537)
Malignant atrophic papulosis (Orphanet:679)
Maturity-onset diabetes of the young, type 3 (OMIM:600496)
Noonan syndrome with multiple lentigines (Orphanet:500)
Polyarteritis nodosa (Orphanet:767)
Polycythemia vera (Orphanet:729)
Polymyositis (Orphanet:732)
Primary familial polycythemia (Orphanet:90042)
Primary lipodystrophy (Orphanet:90970)
Primary systemic amyloidosis (Orphanet:314701)
Pseudoxanthoma elasticum (Orphanet:758)
Relapsing polychondritis (Orphanet:728)
Scleroderma (Orphanet:801)
Senile systemic amyloidosis (Orphanet:330001)
Stevens-Johnson syndrome (Orphanet:36426)
TRAPS syndrome (Orphanet:32960)
Takayasu arteritis (Orphanet:3287)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Werner syndrome (Orphanet:902)
Williams syndrome (Orphanet:904)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)