EAPP, E2F associated phosphoprotein, 55837

N. diseases: 1; N. variants: 0
Disease: Holoprosencephaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly 		0.010 Biomarker disease BEFREE We focused on three genes, SNX6, NPAS3, and C14ORF11, as potential candidates for HPE. 15820313 2005