Premature coronary artery disease
Symptom Information:
Symptom ID: | HPO:0005181 | ||
Synonyms: |
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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) Abnormality of the systemic arterial tree(HPO:0011004) Abnormality of the coronary arteries(HPO:0006704) Coronary artery disease(HPO:0001677) Premature coronary artery disease(HPO:0005181) Abnormalities of the peripheral arteries(HPO:0005114) Arterial stenosis(HPO:0100545) Coronary artery disease(HPO:0001677) Premature coronary artery disease(HPO:0005181) Arteriosclerosis(HPO:0002634) Atherosclerosis(HPO:0002621) Coronary artery disease(HPO:0001677) Premature coronary artery disease(HPO:0005181) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
AORTIC ANEURYSM, FAMILIAL THORACIC 6 | (OMIM:611788) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
MORBID OBESITY AND SPERMATOGENIC FAILURE | (OMIM:615703) |
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism | (Orphanet:280679) |
Tangier disease | (Orphanet:31150) |