tricuspid atresia

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Information
Disease name
tricuspid atresia
Disease ID
DOID:0080169
Description
"A tricuspid valve disease characterized by a missing or abnormally developed tricuspid heart value at birth." [url:https\://medlineplus.gov/ency/article/001110.htm]
Disease area statistics
Chromosome band
Gene symbol Chromosome Start Stop The number of variant
TBX5 12 114,353,931 114,408,442 8
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT01292551 Completed Phase 2 Study of Placebo or Bosentan to Treat Patients With Single Ventricle Physiology. February 2011 March 2013
NCT00507819 Completed Phase 2 Sildenafil After the Fontan Operation December 2007 July 2009
NCT00571233 Completed Biomarker Study for Heart Failure in Children With Single Ventricle Physiology February 2007 January 2015
NCT00573066 Completed Phase 1 Understanding Dexmedetomidine In Infants Post-Operative From Cardiac Surgery May 2004 October 2006
NCT00974025 Completed N/A Impact of Vitamin C on Endothelial Function and Exercise Capacity in Fontan-Palliated Patients June 2009 March 2010
NCT00004828 Completed Phase 1 Liothyronine in Children With Single Ventricle Congenital Cardiac Malformations Undergoing the Fontan Procedure December 1994 December 1997
NCT04467671 Recruiting Phase 2 Two-Year Study of the Safety and Efficacy of the Second-Generation Tissue Engineered Vascular Grafts July 15, 2020 August 2027
NCT04106479 Recruiting NIRS in Congenital Heart Defects - Correlation With Echocardiography October 11, 2019 December 1, 2024
NCT04176458 Terminated N/A Methacetin Breath Test in Patients With Liver Disease Secondary to Heart Disease April 21, 2019 March 19, 2021
NCT01107990 Terminated Global and Regional Myocardial Strain and Power Output In Patients With Single Ventricles Using Novel MRI Techniques November 2009 September 20, 2012
Disase is a (Disease Ontology)
DOID:0050826
Cross Reference ID (Disease Ontology)
GARD:5274
Cross Reference ID (Disease Ontology)
MESH:D018785
Cross Reference ID (Disease Ontology)
MIM:605067
HPO Human Phenotype ID (Human Phenotype Ontology)
HP:0011662
OrphaNumber from OrphaNet (Orphanet)
1209
MeSH unique ID (MeSH (Medical Subject Headings))
D018785