FKBP5, FKBP prolyl isomerase 5, 2289

N. diseases: 179; N. variants: 20
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0021290
Disease: Neonatal disorder
Neonatal disorder
0.300 Biomarker group CTD_human Placental FKBP5 genetic and epigenetic variation is associated with infant neurobehavioral outcomes in the RICHS cohort. 25115650 2014