Phenotypes for disease #05440 (NS9 (Noonan syndrome, type 9 (NS-9)), OMIM:616559)

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000282066 - - Motor delay, Delayed speech and language development, Generalized amyotrophy, Scoliosis, Pectus excavatum, Flexion contracture Unknown 24y - - - - Andreas Laner 00388516
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.