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 |
|
Top Ranked Genes, Molecules or Short Names*
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Top Ranked Key Phrases
Cardio facio cutaneous cfc syndrome ***
 Cardio facio cutaneous syndrome cfc ***
Cardio facio cutaneous syndrome ***
Juvenile myelomonocytic leukemia jmml ***
Protein tyrosine phosphatase shp2 ***
Ras mapk signaling pathway ***
Autosomal dominant disorder characterized ***
Juvenile myelomonocytic leukemia ***
Protein tyrosine phosphatase ***
Autosomal dominant disorder ***
Neurofibromatosis noonan syndrome nfns ***
Autosomal dominant inheritance ***
Acute lymphoblastic leukemia **
Increased nuchal translucency **
Pulmonary valve stenosis **
Congenital heart defect **
Growth hormone therapy **
Genotype phenotype correlations **
Congenital heart disease **
Congenital heart defects **
Genotype phenotype correlation **
Developmental disorder characterized *
Dysmorphic facial features *
Multiple lentigines nsml *
Distinctive facial features *
Characteristic facial features *
Neurofibromatosis noonan syndrome *
Neurofibromatosis type 1 nf1 *
Hypertrophic cardiomyopathy hcm *
Cardiofaciocutaneous cfc syndrome *
Noonan syndrome associated *
Idiopathic short stature *
Noonan syndrome patients n.s.
Cutaneous abnormalities n.s.
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Top Ranked Mesh Terms
Intellectual disability ***
Craniofacial abnormalities ***
Intracellular signaling peptides and proteins ***
Diagnosis differential ***
Retrospective studies ***
Protein tyrosine phosphatase non-receptor type 11 ***
Genetic predisposition to disease ***
Magnetic resonance imaging ***
Dna mutational analysis ***
Genetic association studies ***
Proto-oncogene proteins c-raf ***
Mitogen-activated protein kinases ***
Heart defects congenital ***
Cardiomyopathy hypertrophic ***
Map kinase signaling system ***
Protein tyrosine phosphatases ***
Abnormalities multiple ***
Proto-oncogene proteins p21 ***
Pulmonary valve stenosis ***
Amino acid substitution ***
Tomography x-ray computed **
Leukemia myelomonocytic juvenile **
Ultrasonography prenatal **
Proto-oncogene proteins **
Proto-oncogene proteins b-raf **
Molecular sequence data **
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Top Ranked Mesh Terms (Symptoms)
Intellectual disability ***
Genetic predisposition to disease ***
Urinary bladder neurogenic *
Constriction pathologic *
Sex chromosome aberrations *
Loose anagen hair syndrome *
Fetal growth retardation *
Hearing loss sensorineural *
Postoperative complications n.s.
Language development disorders n.s.
Hypertrophy left ventricular n.s.
Hearing loss conductive n.s.
Death sudden cardiac n.s.
Cell transformation neoplastic n.s.
Translocation genetic n.s.
Chromosomal instability n.s.
Disease susceptibility n.s.
Postoperative hemorrhage n.s.
Neoplasm regression spontaneous n.s.
Ventricular remodeling n.s.
Chromosome inversion n.s.
Subarachnoid hemorrhage n.s.
Yellow nail syndrome n.s.
Ventricular fibrillation n.s.
Hypertrophy right ventricular n.s.
Tachycardia supraventricular n.s.
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