EFHD2, EF-hand domain family member D2, 79180

N. diseases: 29; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 Biomarker phenotype BEFREE A defective function of EFhd2 may also render individuals more prone to the development of psychiatric disorders. 31742960 2019