Disease: HELLP Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162739
Disease: HELLP Syndrome
HELLP Syndrome 		0.030 Biomarker disease BEFREE An association between maternal HELLP syndrome and fetal long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency has been proposed. 17313315 2007
CUI: C0162739
Disease: HELLP Syndrome
HELLP Syndrome 		0.030 GeneticVariation disease BEFREE Because of this, we studied the frequency of the common LCHAD mutation in the Dutch population by analyzing 2,047 Guthrie cards and 113 women who had suffered from HELLP syndrome. 10926288 2000
CUI: C0162739
Disease: HELLP Syndrome
HELLP Syndrome 		0.030 Biomarker disease BEFREE This review explores the causative relationship of a fetal disorder of mitochondrial fatty acid oxidation, long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency, and the serious maternal liver diseases of pregnancy-preeclampsia, the HELLP syndrome (hemolysis, elevated liver enzymes, and low platelet counts), and acute fatty liver of pregnancy. 10331463 1999