Disease: Feeding difficulties ×
Source: CLINVAR ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		0.100 CausalMutation phenotype CLINVAR Germline gain-of-function mutations in SOS1 cause Noonan syndrome. 17143285 2007
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		0.100 CausalMutation phenotype CLINVAR SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome. 17586837 2007
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		0.100 CausalMutation phenotype CLINVAR Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. 17143282 2007