SAA1, serum amyloid A1, 6288

N. diseases: 188; N. variants: 6
Disease: Deficiency of mevalonate kinase ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0342731
Disease: Deficiency of mevalonate kinase
Deficiency of mevalonate kinase 		0.010 GeneticVariation disease BEFREE To determine if SAA concentrations and SAA1 gene polymorphisms could explain the virtual absence of amyloidosis in HIDS patients. 16011988 2005