Phenotypes for disease #03906 (NS8 (Noonan syndrome, type 8 (NS-8)), OMIM:615355)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000060419 Noonan syndrome 8 (OMIM:615355) - - Isolated (sporadic) - - - - - Daniel Trujillano 00080850
0000073481 see paper; ... - - Isolated (sporadic) - - - - - Pia Ostergaard 00043983
0000073482 see paper; ... - - Unknown - - - - - Pia Ostergaard 00043984
0000087499 Osteogenesis imperfecta due to a de novo mutation in COL1A1, heart defect, bronchopulmonal dysplasia, tracheostoma, severe ID, short stature, facial dysmorphism - - Isolated (sporadic) - - - - - Bernt Popp 00111413
0000286549 Cystic hygroma, Fetal cystic hygroma, Edema, Hydrops fetalis, Polyhydramnios, Bilateral fetal pyelectasis, Choroid plexus cyst, Fetal choroid plexus cysts, Abnormality of ductus venosus blood flow, Abnormality of the fetal cardiovascular system 0y - Isolated (sporadic) - - - - - Andreas Laner 00393308
0000304220 Hydrops fetalis, Increased nuchal translucency, Abnormality of ductus venosus blood flow 0y - Unknown - - - - - Andreas Laner 00412206
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