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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
heart disease +    
22q11.2 deletion syndrome +  
anterior spinal artery syndrome 
aortic disease +  
arterial embolism 
arterial occlusion +  
arteriosclerosis disorder +  
Arteritis +  
atrioventricular defect-blepharophimosis-radial and anal defect syndrome 
carcinoid heart disease 
cardiac anomalies-heterotaxy syndrome 
cardiac arrhythmia +  
cardiac edema 
cardiac embolism 
cardiac rhythm disease +  
cardiac tuberculosis 
cardiac ventricle disorder +  
cardiogenetic disease +  
cardiomyopathy +  
cardiotoxicity 
carotid artery disease +  
carotid body paraganglioma +  
cervical artery dissection +  
Churg-Strauss syndrome 
congenital heart disease +  
coronary artery disease +  
An imbalance between myocardial functional requirements and the capacity of the CORONARY VESSELS to supply sufficient blood flow. It is a form of MYOCARDIAL ISCHEMIA (insufficient blood supply to the heart muscle) caused by a decreased capacity of the coronary vessels. Narrowing of the coronary arteries due to fatty deposits inside the arterial walls. Narrowing of the coronary arteries due to fatty deposits inside the arterial walls. The diagnostic criteria may include documented history of any of the following: documented coronary artery stenosis greater than or equal to 50% (by cardiac catheterization or other modality of direct imaging of the coronary arteries); previous coronary artery bypass surgery (CABG); previous percutaneous coronary intervention (PCI); previous myocardial infarction. (ACC) Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. Thickening and loss of elasticity of the CORONARY ARTERIES, leading to progressive arterial insufficiency (CORONARY DISEASE).
Coronary-Subclavian Steal Syndrome 
endocardium disorder +  
fibromuscular dysplasia 
fibromuscular dysplasia, multifocal 
Gerbode defect 
heart aneurysm 
heart conduction disease +  
heart failure +  
Heart neoplasm +  
heart valve disease +  
hypertension +  
hypertensive disorder +  
hypertensive heart disease 
hypotension +  
inflammation of heart layer +  
large artery stroke 
microcephaly-cardiac defect-lung malsegmentation syndrome 
microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type 
Multiple ventricular septal defects 
myocardial disorder +  
pediatric arterial ischemic stroke 
pericardium disorder +  
peripheral arterial disease 
PHACE syndrome 
polyvalvular heart disease syndrome 
post-operative atrial fibrillation 
post-operative myocardial infarction 
pulmonary artery choriocarcinoma 
pulmonary artery leiomyosarcoma 
pulmonary embolism +  
Rare genetic cardiac disease +  
retinal arterial tortuosity 
rheumatic heart disease +  
Single ventricular septal defect 
Sneddon syndrome 
Thomas syndrome 
Ventricular Outflow Obstruction 
white forelock with malformations 

Synonyms
Exact Synonyms: CAD ;   CHD ;   CHD (coronary heart disease) ;   CORONARY ARTERY DIS ;   CORONARY DIS ;   CORONARY HEART DIS ;   Coronary Arterioscleroses ;   Coronary Artery Diseases ;   Coronary Atheroscleroses ;   Coronary Atherosclerosis ;   Coronary Disease ;   Coronary Diseases ;   Coronary Heart Diseases ;   coronary artery disease or disorder ;   coronary artery disorder ;   coronary heart disease ;   disease of coronary artery ;   disease or disorder of coronary artery ;   disorder of coronary artery
Narrow Synonyms: coronary arteriosclerosis
Xrefs: DOID:3393 ;   HP:0001677 ;   ICD10:I25 ;   ICD9:410-414.99 ;   ICD9:414.0 ;   ICD9:414.9 ;   MESH:D003324 ;   MESH:D017202 ;   MONDO:0005010 ;   MedDRA:10011078 ;   NCI:C26732 ;   NCI:C50625 ;   OMIM:608320 ;   OMIM:608901 ;   OMIM:610938 ;   OMIM:614466 ;   OMIM:617347 ;   SCTID:414024009 ;   SCTID:414545008 ;   SNOMEDCT:414545008 ;   SNOMEDCT:443502000 ;   SNOMEDCT:53741008 ;   UMLS:C0151744 ;   UMLS:C1956346
External Ontologys: disease_has_location EFO:UBERON:0000948 ;   disease_has_location EFO:UBERON:0001621 ;   has_disease_location EFO:UBERON:0000948
Definition Sources: NCIT:C26732

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