Myocardial infarction
Symptom Information:
| Symptom ID: | HPO:0001658 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms: |
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| Cross references: |
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| Is a (Direct Parents): |
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| 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) |
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| 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) |