FLVCR2, FLVCR heme transporter 2, 55640

N. diseases: 23; N. variants: 7
Disease: Congenital infectious disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0275544
Disease: Congenital infectious disease
Congenital infectious disease 		0.010 GeneticVariation group BEFREE This case demonstrates the potential clinical utility of testing for mutations in FLVCR2 for patients with hydranencephaly after other possible etiologies, such as congenital infection, have been reasonably eliminated. 25131804 2015