Disease: Hernia, Inguinal ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		0.400 CausalMutation phenotype CLINVAR Arthrogryposis as neonatal presentation of Loeys-Dietz syndrome due to a novel TGFBR2 mutation. 28344185 2017
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		0.400 Biomarker phenotype CTD_human Clinical features in a family with an R460H mutation in transforming growth factor beta receptor 2 gene. 16885183 2006
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		0.400 Biomarker phenotype HPO