RBP4, retinol binding protein 4, 5950

N. diseases: 217; N. variants: 15
Disease: Keratomalacia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0152455
Disease: Keratomalacia
Keratomalacia 		0.300 Biomarker disease CTD_human Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis. 9888420 1999