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QuickView for Noonan syndrome (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. KRAS
  2. HGF
  3. RAF1
  4. SOS1
  5. PTPN11
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. PID_PDGFRB_PATHWAY
  2. PID_GMCSF_PATHWAY
  3. PID_ERBB2_ERBB3_PATHWAY
  4. PID_IL2_1PATHWAY
  5. PID_TRKR_PATHWAY
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Curated Studies

Most Correlated Studies

  1. Mouse Phenotypes - Autosomal dominant hereditary disorder
  2. OMIM - Noonan Syndrome
  3. OMIM - Noonan's syndrome
  4. Pluripotent stem cells and myeloid cells derived and differentiated from Noonan syndrome patients
  5. OMIM - Congenital disorder
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Literature

Most Relevant Literature

  1. Update on Turner and Noonan syndromes.
  2. Ulerythema ophryogenes, a rarely reported cutaneous manifestation of noonan syndrome: case report an…
  3. Extensive abdominal lipomatosis in a patient with Noonan/LEOPARD syndrome (Noonan syndrome-Multiple …
  4. Ulerythema ophryogenes and Noonan syndrome.
  5. Juvenile myelomonocytic leukemia in a 16-year-old with Noonan syndrome: case report.
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Clinical Trials

Most Relevant Clinical Trials

  1. Constitution of a Biological Collection to Study the Pathophysiology in Noonan Syndrome
  2. Study of Metabolic Modifications in Children With Noonan Syndrome
  3. Hormonal Sensitivity in Patients With Noonan and LEOPARD Syndromes
  4. Treatment With HMG-COA Reductase Inhibitor of Growth and Bone Abnormalities in Children With Noonan …
  5. Investigating the Long-term Efficacy and Safety of Two Doses of NN-220 (Somatropin) in Short Stature…
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