Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
Anomalous origin of right coronary artery from the pulmonary artery	HP_0011639	[Right coronary artery begins (branches off from) the pulmonary artery rather than as normal from the root of the aorta, above the right cusp of the aortic valve.]
Partial right sided absence of pericardium	HP_0011632	[A congenital anomaly with lack of part of the pericardium on the righthand side of the heart.]
Complete left sided absence of pericardium	HP_0011633	[A congenital anomaly with complete lack of the pericardium on the lefthand side of the heart.]
Complete diaphragmatic absence of pericardium	HP_0011630	[No pericardium over the diaphragmatic surface of the heart. It is a congenital defect, not the result of a pericardectomy. Pericardium is present on other parts of the heart.]
Complete right sided absence of pericardium	HP_0011631	[No pericardium is present on the righthand side of the heart. It is a congenital absence of pericardium rather than the result of a pericardectomy.]
fetal stage	HsapDv_0000037	[Prenatal stage that starts with the fully formed embryo and ends at birth.]
Postductal coarctation of the aorta	HP_0011647	[Narrowing or constriction of the aorta localized distal to the ductus arteriosus, i.e., to the postductal region of aortic arch.]
Patent ductus arteriosus after birth at term	HP_0011648	[Abnormal persistent patency of the ductus arteriosus in postnatal life when birth was at 37 completed weeks of gestation or greater.]
Dilatation of the sinus of Valsalva	HP_0011645	[Abnormal outpouching or sac-like dilatation of one of the anatomic dilations of the ascending aorta, which occurs just above the aortic valve.]
Juxtaductal coarctation of the aorta	HP_0011646	[Narrowing or constriction of the aorta localized at the insertion of the ductus arteriosus, i.e., to the juxtaductal region of aortic arch.]
Patent ductus arteriosus after premature birth	HP_0011649	[Abnormal persistent patency of the ductus arteriosus when birth was at less than 37 weeks completed gestation.]
Single coronary artery origin	HP_0011640	[The presence of a single coronary artery ostium from which both coronary arteries arise.]
Coronary sinus atrial septal defect	HP_0011643	[An atrial septal defect characterized by a deficiency in the tissue separating the coronary sinus from the left atrium (LA). This results in partial or complete unroofing of the coronary sinus leading to a predominantly left-to-right shunt through the coronary sinus (LA to coronary sinus to right atrium [RA]). The orifice of the ostium is frequently large because of the increased flow. From the RA side, the defect is located at the level of the coronary sinus ostium and may also include some deficiency in atrial tissue around the ostium. From the LA side, the size can be variable depending on the degree of unroofing of the coronary sinus.]
Abnormal coronary sinus morphology	HP_0011642	[An abnormality of the coronary sinus, which is formed by the union of the great cardiac vein and the left marginal vein and terminates in the right atrium. The coronary sinus functions to o collect deoxygenated blood from the myocardium of the heart and drain it into the right atrium.]
Coronary sinus diverticulum	HP_0011644	[A venous pouch within the left ventricular wall, with a neck opening into the coronary sinus.]
Three rows of eyelashes	HP_0008009
obsolete Progressive central visual loss	HP_0008008
Primary congenital glaucoma	HP_0008007
Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis	HP_0011658	[A double outlet right ventricle with a ventricular spetal defect (a hole between the two bottom chambers (ventricles) of the heart), that is considered to be closely related to the pulmonary origin. There is not associated pulmonary stenosis, the abnormal narrowing or constriction of the pulmonary artery, in the main pulmonary artery and/or in the left or right pulmonary artery branches.]
Congenital corneal dystrophy	HP_0008005