Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 335
Gene Symbol: APOA1
APOA1
CUI: C4087498
Disease: Familial LCAT deficiency
Familial LCAT deficiency 		0.300 Biomarker GENOMICS_ENGLAND Possible induction of renal dysfunction in patients with lecithin:cholesterol acyltransferase deficiency by oxidized phosphatidylcholine in glomeruli. 10073988

1999