Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Any direct membership
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Tachycardia, Reciprocating Abnormally rapid heartbeats caused by reentrant conduction over the accessory pathways between the HEART ATRIA and the HEART VENTRICLES. The impulse … | Pathologic Condition | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140082 |
| Tachycardia, Sinoatrial Nodal Reentry Abnormally rapid heartbeats caused by reentry circuit in or around the SINOATRIAL NODE. It is characterized by sudden onset and offset episodes of ta… | Pathologic Condition | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140084 |
| Tachycardia, Sinus Simple rapid heartbeats caused by rapid discharge of impulses from the SINOATRIAL NODE, usually between 100 and 180 beats/min in adults. It is charac… | Pathologic Condition | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140088 |
| Tachycardia, Supraventricular A generic expression for any tachycardia that originates above the BUNDLE OF HIS. | Pathologic Condition | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140085 |
| Tachycardia, Ventricular An abnormally rapid ventricular rhythm usually in excess of 150 beats per minute. It is generated within the ventricle below the BUNDLE OF HIS, eithe… | Pathologic Condition | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140089 |
| Takayasu Arteritis A chronic inflammatory process that affects the AORTA and its primary branches, such as the brachiocephalic artery (BRACHIOCEPHALIC TRUNK) and CAROTI… | Inflammatory Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140220 |
| Takotsubo Cardiomyopathy A transient left ventricular apical dysfunction or ballooning accompanied by electrocardiographic (ECG) T wave inversions. This abnormality is associ… | Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140114 |
| Telangiectasia, Hereditary Hemorrhagic An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. T… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140263 |
| Telangiectasis Permanent dilation of preexisting blood vessels (CAPILLARIES; ARTERIOLES; VENULES) creating small focal red lesions, most commonly in the skin or muc… | Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140284 |
| Tetralogy of Fallot A combination of congenital heart defects consisting of four key features including VENTRICULAR SEPTAL DEFECTS; PULMONARY STENOSIS; RIGHT VENTRICULAR… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140034 |
| Thromboangiitis Obliterans A non-atherosclerotic, inflammatory thrombotic disease that commonly involves small and medium-sized arteries or veins in the extremities. It is char… | Vascular Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140234 |
| Thromboembolism Obstruction of a blood vessel (embolism) by a blood clot (THROMBUS) in the blood stream. | Vascular Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140244 |
| Thromboinflammation Thrombosis with associated inflammation due to crosstalk between HEMOSTASIS and INNATE IMMUNE RESPONSES modulated by PLATELETS. It is associated with… | Vascular Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140251 |
| Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | Vascular Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140254 |
| Thrombosis The label denotes a pathological biological process or mechanism, not a disease entity. | Pathological process | Pathology | Cardiovascular System [curated_secondary] | AMW:PROC:125025 |
| Torsades de Pointes A malignant form of polymorphic ventricular tachycardia that is characterized by HEART RATE between 200 and 250 beats per minute, and QRS complexes w… | Pathologic Condition | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140091 |
| Transmural Myocardial Infarction Created as a target node for a staged ClinicalGraph edge. Review and enrich this node later if needed. | Vascular Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140309 |
| Transposition of Great Vessels A congenital cardiovascular malformation in which the AORTA arises entirely from the RIGHT VENTRICLE, and the PULMONARY ARTERY arises from the LEFT V… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140035 |
| Tricuspid Atresia Absence of the orifice between the RIGHT ATRIUM and RIGHT VENTRICLE, with the presence of an atrial defect through which all the systemic venous retu… | Pathologic Condition | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140037 |
| Tricuspid Valve Insufficiency Backflow of blood from the RIGHT VENTRICLE into the RIGHT ATRIUM due to imperfect closure of the TRICUSPID VALVE. | Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140146 |
| Tricuspid Valve Prolapse Abnormal protrusion of one or more of the leaflets of TRICUSPID VALVE into the RIGHT ATRIUM during SYSTOLE. This allows the backflow of blood into ri… | Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140140 |
| Tricuspid Valve Stenosis The pathologic narrowing of the orifice of the TRICUSPID VALVE. This hinders the emptying of RIGHT ATRIUM leading to elevated right atrial pressure a… | Pathologic Condition | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140147 |
| Trilogy of Fallot A combination of congenital heart defects consisting of three key features including ATRIAL SEPTAL DEFECTS; PULMONARY STENOSIS; and RIGHT VENTRICULAR… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140038 |
| Trisomy 18 Syndrome A chromosome disorder associated with TRISOMY of all or part of CHROMOSOME 18. Clinical manifestations include INTRAUTERINE GROWTH RETARDATION; CLEFT… | Syndrome | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140039 |
| Truncus Arteriosus, Persistent A congenital anomaly caused by the failed development of TRUNCUS ARTERIOSUS into separate AORTA and PULMONARY ARTERY. It is characterized by a single… | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140022 |
| Univentricular Heart Rare congenital heart malformation with a single ventricle (HEART VENTRICLES) instead of the usual two. | Congenital Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140040 |
| Upper Extremity Deep Vein Thrombosis The label is process-shaped, but the organ-specific concept may also function as a disorder; manual semantic review is required. | Pathological process | Pathology | Cardiovascular System [role_derived] | AMW:PROC:125043 |
| Valvular Aortic Stenosis Valvular aortic stenosis used as a ClinicalGraph target concept for pathology / differential. | Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140305 |
| Varicose Ulcer Skin breakdown or ulceration in the drainage area of a VARICOSE VEIN, usually in the leg. | Pathologic Condition | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140286 |
| Varicose Veins Enlarged and tortuous VEINS. | Disorder | Pathology | Cardiovascular System [curated_secondary] | AMW:DIS:140285 |