Double Outlet Right Ventricle (DORV)

Alias:

Double Outlet Right Ventricle with Subpulmonary Ventricular Septal Defect

Taussig-Bing Syndrome

Dorv

Double Outlet Right Ventricle with Subaortic or Doubly Committed Interventricular Communication Without Pulmonary Stenosis

Double Outlet Right Ventricle with Subaortic or Doubly Committed Interventricular Communication and Pulmonary Stenosis

Double Outlet Right Ventricle with Subpulmonary Interventricular Communication, Transposition Type

Double Outlet Right Ventricle with Non-Committed Interventricular Communication

Double Outlet Right Ventricle with Uncommitted Ventricular Septal Defect

Double Outlet Right Ventricle with Transposition of the Great Arteries

Double Outlet Right Ventricle with Remote Ventricular Septal Defect

Dorv [double Outlet Right Ventricle]

Taussig-Bing Syndrome or Defect

Dextrotransposition of Aorta

Dorv with Subpulmonary Vsd

Taussig-Bing Malformation

Taussig-Bing Complex

Taussig-Bing Defect

Taussig-Bing Heart

Taussig-Bing

Dorv-Tga

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Double Outlet Right Ventricle, also known as taussig-bing syndrome, is related to conotruncal heart malformations and congenital heart defects, multiple types, 6. An important gene associated with Double Outlet Right Ventricle is NKX2-5 (NK2 Homeobox 5), and among its related pathways/superpathways are Nervous system development and Human Embryonic Stem Cell Pluripotency. The drugs Propranolol and Vasodilator Agents have been mentioned in the context of this disorder. Affiliated tissues include heart and thymus, and related phenotypes are double outlet right ventricle and cyanosis

Related ID：

MALACARDS：DBL002

MESH：D004310

ICD11：1060446859