Phenotypes for disease #00682 (NS3 (Noonan syndrome, type 3 (NS-3)), OMIM:609942)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000073484 see paper; ... - - Unknown - - - - - Pia Ostergaard 00043992
0000073485 see paper; ... - - Unknown - - - - - Pia Ostergaard 00043991
0000087497 Severe speech delay, moderate ID, behavioral anomalies, normal growth, facial dsymorphism, low set ears - - Isolated (sporadic) - - - - - Bernt Popp 00111412
0000308489 Hydronephrosis, Single umbilical artery, Abnormality of prenatal development or birth, Intrauterine growth retardation, Hydrops fetalis, Fetal ascites, Atrioventricular canal defect, Fetal cystic hygroma, Fetal pyelectasis, Fetal hydrothorax prenatal - Isolated (sporadic) - - - - - Andreas Laner 00416979
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