Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Audiological findings in Noonan syndrome. | 27619028 | 2016 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Ocular Manifestations of Noonan Syndrome: A Prospective Clinical and Genetic Study of 25 Patients. | 27521173 | 2016 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Craniosynostosis and Noonan syndrome with KRAS mutations: Expanding the phenotype with a case report and review of the literature. | 26249544 | 2015 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Chronic pain in Noonan Syndrome: A previously unreported but common symptom. | 26297936 | 2015 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes. | 21500339 | 2011 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome. | 21533187 | 2011 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Noonan syndrome and clinically related disorders. | 21396583 | 2011 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. | 19206169 | 2009 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | The RASopathies: developmental syndromes of Ras/MAPK pathway dysregulation. | 19467855 | 2009 | |||||
Noonan Syndrome
|
0.700 | CausalMutation | CLINVAR | PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome. | 19020799 | 2008 | |||||
Noonan Syndrome
|
0.700 | CausalMutation | CLINVAR | Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients. | 18331608 | 2008 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Noonan syndrome. | 17222357 | 2007 | |||||
Noonan Syndrome
|
0.700 | CausalMutation | CLINVAR | Mutational analysis of PTPN11 gene in Taiwanese children with Noonan syndrome. | 17339163 | 2007 | |||||
Noonan Syndrome
|
0.700 | CausalMutation | CLINVAR | Mutation analysis of the genes involved in the Ras-mitogen-activated protein kinase (MAPK) pathway in Korean patients with Noonan syndrome. | 17661820 | 2007 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations. | 17056636 | 2007 | |||||
Noonan Syndrome
|
0.700 | CausalMutation | CLINVAR | PTPN11 gene analysis in 74 Brazilian patients with Noonan syndrome or Noonan-like phenotype. | 17020470 | 2006 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | LEOPARD syndrome: clinical diagnosis in the first year of life. | 16523510 | 2006 | |||||
Curly hair (finding)
|
0.700 | CausalMutation | CLINVAR | Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia. | 15834506 | 2005 | |||||
Noonan Syndrome
|
0.700 | CausalMutation | CLINVAR | Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia. | 15834506 | 2005 | |||||
Multiple nevi
|
0.700 | CausalMutation | CLINVAR | Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia. | 15834506 | 2005 | |||||
Congenital ocular coloboma (disorder)
|
0.700 | CausalMutation | CLINVAR | Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia. | 15834506 | 2005 | |||||
Dysmorphic features
|
0.700 | CausalMutation | CLINVAR | Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes. | 12960218 | 2003 | |||||
Noonan Syndrome
|
0.700 | CausalMutation | CLINVAR | PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. | 11992261 | 2002 | |||||
Multiple nevi
|
0.700 | CausalMutation | CLINVAR | Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. | 11704759 | 2001 | |||||
Curly hair (finding)
|
0.700 | CausalMutation | CLINVAR | Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. | 11704759 | 2001 |