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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
Use Cases
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
eRAM
DisGeNET
High level summary of knowledge for a disease, including descriptions and datasource references.