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cardiac septal defects
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
MEIS2
EPHB4
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
positive regulation of cardiac muscle myoblast proliferation
FAN_EMBRYONIC_CTX_EX_1_EXCITATORY_NEURON
PLASARI_TGFB1_TARGETS_1HR_DN
SEF1_C
Homeobox protein PKNOX/Meis, N-terminal
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Curated Studies
Most Correlated Studies
OMIM - Facial cleft
OMIM - Hydrops fetalis
OMIM - Multisystem Complex Disorders
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Literature
Most Relevant Literature
Screening and evaluation of TBX20 and CITED2 mutations in children with congenital cardiac septal de…
Mutational Assessment in NKX2-5 and ACTC1 Genes in Patients with Congenital Cardiac Septal Defect (C…
General Anesthesia With Remimazolam During Minimally Invasive Cardiac Surgery for Atrial Septal Defe…
Familial cardiac septal defect due to a novel nine-base deletion in TBX20.
Progress of biodegradable polymer application in cardiac occluders.
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Clinical Trials
Most Relevant Clinical Trials
Transcatheter Closure Versus Surgery of Perimembranous Ventricular Septal Defects
A Randomized Controlled Trial:Treatments on Infundibular Ventricular Septal Defect
Transcatheter Versus Surgical Closure of Ventricular Septal Defect: A Comparative Study
Cardiopulmonary Function in Adults Born With a Ventricular Septal Defect
Closure of Muscular Ventricular Septal Defects With The AMPLATZERâ„¢ Muscular VSD Occluder
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