Angina pectoris
Symptom Information:
Symptom ID: | HPO:0001681 | |||||||||||||||||||||||||||||||||||||
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) Abnormality of the systemic arterial tree(HPO:0011004) Abnormality of the coronary arteries(HPO:0006704) Coronary artery disease(HPO:0001677) Angina pectoris(HPO:0001681) Abnormalities of the peripheral arteries(HPO:0005114) Arterial stenosis(HPO:0100545) Coronary artery disease(HPO:0001677) Angina pectoris(HPO:0001681) Arteriosclerosis(HPO:0002634) Atherosclerosis(HPO:0002621) Coronary artery disease(HPO:0001677) Angina pectoris(HPO:0001681) MedDRA: Vascular disorders(MedDRA:10047065) Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216) Coronary necrosis and vascular insufficiency(MedDRA:10065875) Angina pectoris(HPO:0001681) |
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Database Frequency: | 22 / 7739 | |||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
APOLIPOPROTEIN E | (OMIM:107741) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Cardiomyopathy, familial hypertrophic, 3 | (OMIM:115196) |
Cardiomyopathy, familial hypertrophic, 4 | (OMIM:115197) |
Cardiomyopathy, hypertrophic, 25 | (OMIM:607487) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
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) |
Fish-eye disease | (Orphanet:79292) |
HEPATIC LIPASE DEFICIENCY | (OMIM:614025) |
Heritable pulmonary arterial hypertension | (Orphanet:275777) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
Idiopathic pulmonary arterial hypertension | (Orphanet:275766) |
PSEUDOXANTHOMA ELASTICUM, FORME FRUSTEPSEUDOXANTHOMA ELASTICUM, HETEROZYGOUS, INCLUDED | (OMIM:177850) |
PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:265400) |
Papillary fibroelastoma of the heart | (Orphanet:208600) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Werner syndrome | (Orphanet:902) |
[DEL] PSEUDOXANTHOMA ELASTICUM | (OMIM:264800) |