Phenotypes for disease #00641 (NS7 (Noonan syndrome, type 7 (NS-7)), OMIM:613706)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000073486 see paper; ... - - Isolated (sporadic) - - - - - Pia Ostergaard 00043993
0000291838 Failure to thrive, Abnormal hepatic echogenicity, Proptosis, Hypertonia, Low-set ears, High forehead - - Isolated (sporadic) 00y07m - - - - Andreas Laner 00398754
0000302535 - - - Familial, autosomal dominant - - - - - Simin Zheng 00410430
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