Angina pectoris

Symptom Information:

Symptom ID: HPO:0001681
Synonyms:
Angina (disorder) [Orphanet:35090]
Ischemic chest pain (finding) [Orphanet:35090]
Angina Pectoris [Orphanet:35090]
Angina pectoris [OMIM:Angina pectoris]
Angor pectoris/myocardial infarction [Orphanet:35090]
Angina pectoris [Orphanet:35090]
Angina pectoris [MedDRA:10002383]
Angina [MedDRA:10002383]
Angina aggravated [MedDRA:10002383]
Angina attack [MedDRA:10002383]
Angina of effort [MedDRA:10002383]
Angina on exercise [MedDRA:10002383]
Angina pectoris aggravated [MedDRA:10002383]
Angina symptom [MedDRA:10002383]
Angina syndrome [MedDRA:10002383]
Angina worsened [MedDRA:10002383]
Anginal attack [MedDRA:10002383]
Anginal pain [MedDRA:10002383]
Anginal syndrome [MedDRA:10002383]
Cardialgia [MedDRA:10002383]
Chest pain - cardiac [MedDRA:10002383]
Effort angina [MedDRA:10002383]
Elsner's asthma [MedDRA:10002383]
Exercise induced angina [MedDRA:10002383]
Heberden's angina [MedDRA:10002383]
Increased angina [MedDRA:10002383]
Other and unspecified angina pectoris [MedDRA:10002383]
Rougnon-Heberden disease [MedDRA:10002383]
Stenocardia [MedDRA:10002383]
Stable angina pectoris [MedDRA:10002383]
Anginal discomfort [MedDRA:10002383]
Cardiac pain [MedDRA:10002383]
Ischaemic chest pain [MedDRA:10002383]
Ischemic chest pain [MedDRA:10002383]
Atypical angina [MedDRA:10002383]
Refractory angina pectoris [MedDRA:10002383]
Angina [OMIM:Angina]
Quality:
Cross references:
Orphanet:35090 "Angor pectoris/myocardial infarction" [Orphanet:35090]
OMIM: "Angina pectoris" [OMIM:Angina pectoris]
OMIM: "Angina" [OMIM:Angina]
UMLS:C0002962 "Angina Pectoris" [Orphanet:35090]
Is a (Direct Parents):
HPO         Coronary artery disease
Orphanet Abnormality of cardiovascular system physiology
Orphanet Myocardial infarction
MedDRA Coronary necrosis and vascular insufficiency
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)
                Abnormalities of the peripheral arteries(HPO:0005114)
                   Arterial stenosis(HPO:0100545)
                      Coronary artery disease(HPO:0001677)
                         Angina pectoris(HPO:0001681)
                Abnormality of the coronary arteries(HPO:0006704)
                   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)
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)