FABP2, fatty acid binding protein 2, 2169

N. diseases: 65; N. variants: 2
Disease: Cerebrovascular Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		0.030 GeneticVariation group BEFREE Both asymmetric dimethylarginine (ADMA), which is an inhibitor of endothelial nitric oxide synthase and the fatty acid-binding protein 2 (FABP2) A54T gene polymorphism have been associated with cerebrovascular disease. 17212611 2007
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		0.030 Biomarker group BEFREE The alanine (A) to threonine (T) substitution at codon 54 of the intestinal fatty acid-binding protein 2 (FABP2) has been associated with dyslipidaemia and other characteristics of the metabolic syndrome, which in turn is a risk factor for cerebrovascular disease. 16013194 2005
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		0.030 GeneticVariation group BEFREE The FABP2 gene polymorphism in cerebrovascular disease. 15527447 2004