FLVCR2, FLVCR heme transporter 2, 55640

N. diseases: 23; N. variants: 7
Disease: Hydranencephaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020225
Disease: Hydranencephaly
Hydranencephaly 		0.110 GeneticVariation disease BEFREE Current literature on FLVCR2 is relatively sparse; identifying additional patients with similar mutations will aid in defining the clinical significance of a gene mutation and the contribution to the etiology of hydranencephaly. 25131804 2015
CUI: C0020225
Disease: Hydranencephaly
Hydranencephaly 		0.110 Biomarker disease HPO