RBP4, retinol binding protein 4, 5950

N. diseases: 217; N. variants: 15
Disease: Retinol Deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0856901
Disease: Retinol Deficiency
Retinol Deficiency 		0.310 GeneticVariation disease BEFREE Biochemical basis for retinol deficiency induced by the I41N and G75D mutations in human plasma retinol-binding protein. 16157297 2005
CUI: C0856901
Disease: Retinol Deficiency
Retinol Deficiency 		0.310 Biomarker disease CTD_human Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis. 9888420 1999