Pick one of the followings
*Some genes may be words of complete meaning. In any case, if present, they are relevant key words.
Legend:
*** | p-value <= 0.001 |
** | p-value <= 0.01 |
* | p-value <= 0.05 |
n.s. | not significant |
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Top Ranked Genes, Molecules or Short Names*
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Top Ranked Key Phrases
Velo cardio facial syndrome vcfs ***
Velo cardio facial syndrome ***
T box transcription factor ***
Right sided aortic arch ***
Conotruncal anomaly face syndrome ***
Congenital heart disease chd ***
Severe combined immunodeficiency scid ***
Situ hybridization fish analysis ***
Left subclavian artery ***
Interrupted aortic arch ***
Ventricular septal defect ***
Cardiac outflow tract ***
Congenital heart disease **
Conotruncal heart defects **
Congenital heart defects **
Pharyngeal arch arteries **
Persistent truncus arteriosus **
Severe combined immunodeficiency **
Complete digeorge syndrome **
Situ hybridization fish **
Fourth pharyngeal pouches **
Partial digeorge syndrome **
Chromosomal region 22q11 **
Velocardiofacial syndrome vcfs **
2 deletion syndrome 22q11ds *
Common microdeletion syndrome *
2 deletion syndrome 22q11 *
22q11 deletion syndrome *
Chromosome 22q11 deletion *
Digeorge syndrome patients *
Primary immunodeficiency n.s.
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Top Ranked Mesh Terms
Immunologic deficiency syndromes ***
T-box domain proteins ***
Abnormalities multiple ***
Molecular sequence data ***
Translocation genetic ***
Heart defects congenital ***
Transcription factors ***
Chromosomes human pair 22 ***
Disease models animal ***
Gene expression regulation developmental ***
Retrospective studies ***
Chromosome aberrations ***
In situ hybridization fluorescence ***
Sequence homology amino acid ***
Severe combined immunodeficiency ***
Magnetic resonance imaging **
Craniofacial abnormalities **
Ultrasonography prenatal **
Heart septal defects ventricular **
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Top Ranked Mesh Terms (Symptoms)
Translocation genetic ***
Chromosome aberrations ***
Intellectual disability *
Genetic predisposition to disease *
Constriction pathologic *
Retinal neovascularization *
Hernias diaphragmatic congenital *
Chromosome inversion n.s.
Tracheoesophageal fistula n.s.
Postoperative complications n.s.
Hearing loss sensorineural n.s.
Fetal growth retardation n.s.
Chromosome duplication n.s.
Hypertrophy left ventricular n.s.
Cell transformation viral n.s.
Hernia diaphragmatic n.s.
Purpura thrombocytopenic idiopathic n.s.
Pigmentation disorders n.s.
Hearing loss conductive n.s.
Chromosome fragility n.s.
Nondisjunction genetic n.s.
Psychomotor disorders n.s.
Multiple organ failure n.s.
Graft occlusion vascular n.s.
Sex chromosome aberrations n.s.
Language development disorders n.s.
Cell transformation neoplastic n.s.
Neovascularization pathologic n.s.
Neoplasm invasiveness n.s.
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