Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5950
Gene Symbol: RBP4
RBP4
CUI: C0856901
Disease: Retinol Deficiency
Retinol Deficiency 		0.310 Biomarker CTD_human Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis. 9888420

1999