rs121918455, PTPN11

N. diseases: 31
Disease: Septal hypertrophy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Septal hypertrophy
CUI: C0442887
Disease: Septal hypertrophy
0.700 CausalMutation CLINVAR Genotype differences in cognitive functioning in Noonan syndrome. 19077116 2009
Septal hypertrophy
CUI: C0442887
Disease: Septal hypertrophy
0.700 CausalMutation CLINVAR Noonan syndrome and related disorders: genetics and pathogenesis. 16124853 2005
Septal hypertrophy
CUI: C0442887
Disease: Septal hypertrophy
0.700 CausalMutation CLINVAR Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes. 12960218 2003
Septal hypertrophy
CUI: C0442887
Disease: Septal hypertrophy
0.700 CausalMutation CLINVAR PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. 11992261 2002