ALB, albumin, 213

N. diseases: 1198; N. variants: 21
Disease: Dysalbuminemic Hyperthyroxinemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1863119
Disease: Dysalbuminemic Hyperthyroxinemia
Dysalbuminemic Hyperthyroxinemia 		0.010 GeneticVariation disease BEFREE A novel mutation (R222I) in the ALB gene mediates dominantly inherited dysalbuminemic hyperthyroxinemia. 24646103 2014