eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | noonan syndrome |
| Symptom | C0010278|craniosynostosis |
| Sentences | 1 |
| PubMedID- 25123707 | Severe craniosynostosis with noonan syndrome phenotype associated with shoc2 mutation: clinical evidence of crosslink between fgfr and ras signaling pathways. |
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