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Saldino-Noonan syndrome

Disease Summary
Associated Targets (13)
Tbio

12

Tchem

1


Disease Ontology Description A syndrome characterized by congenital heart defects, failure to thrive, short stature, cognitive dysfunction, pectus excavatum, coagulation defects and craniofacial defects, has_material_basis_in the mutation in the Ras/mitogen activated protein kinase.
DataSource References
eRAM:  DOID:0050549
DisGeNET:  UMLS:C0036069