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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
8q24.3 microdeletion syndrome 
Alagille syndrome +  
alveolar capillary dysplasia with misalignment of pulmonary veins 
aneurysm  
Aneurysm, False 
angioosteohypertrophic syndrome 
aortic valve atresia 
arterial calcification of infancy +  
arterial disorder +   
arterial occlusive disease +   
arterial tortuosity syndrome 
Arterio-Arterial Fistula 
atrial conduction disease 
atrial heart septal defect +   
atrioventricular block +   
autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome 
Bannayan-Riley-Ruvalcaba syndrome 
bleeding disorder, vascular-type 
blood vessel injury 
blood vessel neoplasm +   
Brugada syndrome +   
capillary disorder +  
capillary malformation +  
cardiac anomalies - developmental delay - facial dysmorphism syndrome 
cardiac embolism  
cardiac valvular dysplasia, X-linked 
cerebral arteriopathy with subcortical infarcts and leukoencephalopathy +  
Char syndrome 
CHARGE syndrome 
CHIME syndrome 
cholesterol embolism +  
COG1-congenital disorder of glycosylation 
congenital heart defects, multiple types +  
congenital heart defects, multiple types, 3 
congenital heart defects, multiple types, 5 
congenital heart malformation +   
congenital pulmonary veins anomaly +  
congenital vertebral-cardiac-renal anomalies syndrome +  
coronary artery disease, autosomal dominant 2 
Coronary-Subclavian Steal Syndrome 
dextro-looped transposition of the great arteries +  
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 
Ehlers-Danlos syndrome, cardiac valvular type 
Ehlers-Danlos syndrome, musculocontractural type 
Ehlers-Danlos syndrome, vascular type +  
Ehlers-Danlos syndrome, vascular-like type 
Ellis-van Creveld syndrome 
Embolism, Paradoxical 
endothelial dysfunction 
epistaxis 
familial atrial fibrillation +  
familial atrial myxoma 
familial atrioventricular septal defect +  
familial bicuspid aortic valve 
familial cardiomyopathy +  
familial long QT syndrome +   
familial retinal arterial macroaneurysm 
familial sick sinus syndrome +   
familial thoracic aortic aneurysm and aortic dissection +  
GATA5-related congenital heart defects +  
GATA6-related congenital heart disease with or without pancreatic agenesis or neonatal diabetes +  
heart defects-limb shortening syndrome 
heart septal defect +   
Hemangiopericytic Neoplasm +  
hepatic vascular disorder +   
Hepatopulmonary Syndrome 
hereditary arterial and articular multiple calcification syndrome 
Holt-Oram syndrome +  
hypoplastic left heart syndrome +  
inherited mitral valve disease +  
ischemic colitis 
ischemic disease +   
Larsen-like syndrome, B3GAT3 type 
left ventricular noncompaction +  
lethal arteriopathy syndrome due to fibulin-4 deficiency 
LMNA-related cardiocutaneous progeria syndrome 
Loeys-Dietz syndrome +  
lymphatic malformation +  
lymphatic vessel neoplasm +   
macrovascular complications of diabetes  
MGAT2-congenital disorder of glycosylation 
mitral atresia disorder 
multiple cutaneous and mucosal venous malformations 
multisystemic smooth muscle dysfunction syndrome 
neonatal Marfan syndrome 
neurovascular disorder +   
ocular vascular disease +   
orthostatic intolerance 
patent ductus arteriosus 2 
patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome 
PDA1 
pericardial effusion, chronic 
peripheral vascular disease +   
persistent truncus arteriosus 
Peters plus syndrome 
progressive familial heart block +  
pulmonary hypertension, primary, autosomal recessive 
pulmonary venoocclusive disease +  
renal nutcracker syndrome 
Sengers syndrome 
severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome 
short QT syndrome +  
sinoatrial node dysfunction and deafness 
skin vascular disease +   
small artery occlusion  
STING-associated vasculopathy with onset in infancy 
structural congenital heart disease, multiple types - GATA4 +  
Superior Vena Cava Syndrome 
supravalvular aortic stenosis 
Systemic capillary leak syndrome 
TARP syndrome 
thoracic outlet syndrome +  
thrombotic disease +   
transketolase deficiency 
tricuspid atresia 
vascular anomaly +  
vascular disorder of penis 
vascular ectasia +  
vascular hemostatic disease +  
vascular insufficiency disorder +   
vascular malformation +  
vascular occlusion disorder +  
vascular toxicity 
vasculitis +   
vein disorder +   
venous thromboembolism  
ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome 
ventricular fibrillation, paroxysmal familial, type 1 
ventricular septal defect +  
ventricular tachycardia, familial +  

Synonyms
Exact Synonyms: PDA2 ;   patent ductus arteriosus 2; PDA2 ;   patent ductus arteriosus type 2
Alternate IDs: MONDO:0014878
Xrefs: GARD:18489 ;   MEDGEN:924886 ;   MIM:617035 ;   UMLS:C4284595

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