Myocardial infarction

Symptom Information:

Symptom ID: HPO:0001658
Synonyms:
Acute coronary syndrome [Orphanet:35090]
Myocardial infarction (disorder) [Orphanet:35090]
Acute coronary syndrome (disorder) [Orphanet:35090]
Myocardial Infarction [Orphanet:35090]
Acute Coronary Syndrome [Orphanet:35090]
Myocardial infarction [OMIM:Myocardial infarction]
Angor pectoris/myocardial infarction [Orphanet:35090]
Myocardial infarction [Orphanet:35090]
Myocardial infarction [MedDRA:10028596]
Anterior MI [MedDRA:10028596]
Attack heart (NOS) [MedDRA:10028596]
Cardiopathy necrotic [MedDRA:10028596]
Certain sequelae of myocardial infarction, not elsewhere classified [MedDRA:10028596]
Heart attack [MedDRA:10028596]
Infarct myocardial [MedDRA:10028596]
Inferior MI [MedDRA:10028596]
MI [MedDRA:10028596]
Myocardial infarct [MedDRA:10028596]
Myocardial infarction old [MedDRA:10028596]
Myocardial infarction old healed [MedDRA:10028596]
Myocardial necrosis [MedDRA:10028596]
Necrosis myocardium [MedDRA:10028596]
Non-Q wave MI [MedDRA:10028596]
Old myocardial infarction [MedDRA:10028596]
Other sequelae of myocardial infarction, not elsewhere classified [MedDRA:10028596]
Post MI [MedDRA:10028596]
Q wave MI [MedDRA:10028596]
Anteroseptal infarction [MedDRA:10028596]
Anteroseptal necrosis [MedDRA:10028596]
Myocardial reinfarction [MedDRA:10028596]
Age indeterminate myocardial infarction [MedDRA:10028596]
Age indeterminate anterior myocardial infarction [MedDRA:10028596]
Age indeterminate inferior myocardial infarction [MedDRA:10028596]
Age indeterminate lateral myocardial infarction [MedDRA:10028596]
Age indeterminate posterior myocardial infarction [MedDRA:10028596]
Subendocardial myocardial infarction [MedDRA:10028596]
Age indeterminate anteroseptal myocardial infarction [MedDRA:10028596]
Age indeterminate posterolateral myocardial infarction [MedDRA:10028596]
Age indeterminate septal myocardial infarction [MedDRA:10028596]
Age indeterminate inferolateral myocardial infarction [MedDRA:10028596]
Age indeterminate inferoposterior myocardial infarction [MedDRA:10028596]
Anterior myocardial infarction [MedDRA:10028596]
Inferior myocardial infarction [MedDRA:10028596]
Lateral myocardial infarction [MedDRA:10028596]
Posterior myocardial infarction [MedDRA:10028596]
Septal myocardial infarction [MedDRA:10028596]
Posterolateral myocardial infarction [MedDRA:10028596]
Inferolateral myocardial infarction [MedDRA:10028596]
Inferposterial myocardial infarction [MedDRA:10028596]
Age indeterminate right ventricular infarction [MedDRA:10028596]
Age indeterminate anterolateral myocardial infarction [MedDRA:10028596]
Posteroinferior myocardial infarction [MedDRA:10028596]
Apical myocardial infarction [MedDRA:10028596]
Transmural myocardial infarction [MedDRA:10028596]
Anterolateral myocardial infarction [MedDRA:10028596]
Acute coronary syndrome [MedDRA:10051592]
Attack coronary [MedDRA:10051592]
Non ST segment elevation acute coronary syndrome [MedDRA:10051592]
Myocardial infarction (MI) [OMIM:Myocardial infarction (MI)]
Myocardial infarction (in some patients) [OMIM:Myocardial infarction (in some patients)]
Myocardial infarction (secondary to coronary artery thrombosis) [OMIM:Myocardial infarction (secondary to coronary artery thrombosis)]
Quality:
Cross references:
Orphanet:35090 "Angor pectoris/myocardial infarction" [Orphanet:35090]
OMIM: "Myocardial infarction" [OMIM:Myocardial infarction]
OMIM: "Myocardial infarction (MI)" [OMIM:Myocardial infarction (MI)]
OMIM: "Myocardial infarction (in some patients)" [OMIM:Myocardial infarction (in some patients)]
OMIM: "Myocardial infarction (secondary to coronary artery thrombosis)" [OMIM:Myocardial infarction (secondary to coronary artery thrombosis)]
UMLS:C0027051 "Myocardial Infarction" [Orphanet:35090]
UMLS:C0948089 "Acute Coronary Syndrome" [Orphanet:35090]
Is a (Direct Parents):
MedDRA Coronary necrosis and vascular insufficiency
Orphanet Abnormality of cardiovascular system physiology
HPO         Coronary artery disease
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)
                      Myocardial infarction(HPO:0001658)
             Abnormality of the systemic arterial tree(HPO:0011004)
                Abnormalities of the peripheral arteries(HPO:0005114)
                   Arterial stenosis(HPO:0100545)
                      Coronary artery disease(HPO:0001677)
                         Myocardial infarction(HPO:0001658)
                Abnormality of the coronary arteries(HPO:0006704)
                   Coronary artery disease(HPO:0001677)
                      Myocardial infarction(HPO:0001658)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216)
       Coronary necrosis and vascular insufficiency(MedDRA:10065875)
          Myocardial infarction(HPO:0001658)
Database Frequency: 30 / 7739
Resource:

All diseases associated with this symptom:

ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2 (OMIM:614473)
ARTERIOSCLEROSIS, SEVERE JUVENILE (OMIM:208060)
ATHEROSCLEROSIS SUSCEPTIBILITY (OMIM:108725)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 (OMIM:608320)
Cardiomyopathy, dilated, 1V (OMIM:613697)
Cerebrotendinous xanthomatosis (Orphanet:909)
Classical homocystinuria (Orphanet:394)
Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis (Orphanet:94062)
Fabry disease (Orphanet:324)
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)
Fibromuscular dysplasia of arteries (Orphanet:336)
Fish-eye disease (Orphanet:79292)
Generalized arterial calcification of infancy (Orphanet:51608)
HYPERLIPIDEMIA, FAMILIAL COMBINED (OMIM:144250)
Hurler syndrome (Orphanet:93473)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
MAY-HEGGLIN ANOMALY (OMIM:155100)
MORBID OBESITY AND SPERMATOGENIC FAILURE (OMIM:615703)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
Papillary fibroelastoma of the heart (Orphanet:208600)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Primary familial polycythemia (Orphanet:90042)
Pseudoxanthoma elasticum (Orphanet:758)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Tangier disease (Orphanet:31150)
Werner syndrome (Orphanet:902)