MED1, mediator complex subunit 1, 5469

N. diseases: 88; N. variants: 4
Disease: Erythrophagocytosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0302486
Disease: Erythrophagocytosis
Erythrophagocytosis 		0.010 Biomarker disease BEFREE These defects include the failure of labyrinthine development, the dilation of maternal blood sinuses, the massive erythrophagocytosis by trophoblasts, the alteration of trophoblast populations, and the lower proliferation of myocardium, which are similar to those encountered in mice lacking PPARgamma or the PPARgamma-binding protein (PBP, TRAP220, or DRIP205). 12368298 2002