Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 CausalMutation CLINVAR Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Evaluation of Genotype-Phenotype Correlation in Patients Detected by Newborn Screening. 25940036 2015
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation CLINVAR An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals. 22975760 2013
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation CLINVAR The first three years of screening for medium chain acyl-CoA dehydrogenase deficiency (MCADD) by newborn screening ontario. 21083904 2010
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation CLINVAR Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: under-representation of the common c.985 A > G mutation in the New York state population. 18241067 2008
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation CLINVAR Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations. 16291504 2006
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 CausalMutation CLINVAR Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations. 16291504 2006
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency. 11486912 2001
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency. 11349232 2001
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Molecular and functional characterisation of mild MCAD deficiency. 11409868 2001
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency. 10767181 2000
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Biochemical characterization of a variant human medium-chain acyl-CoA dehydrogenase with a disease-associated mutation localized in the active site. 9882619 1999
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 CausalMutation CLINVAR The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype? 9158144 1997
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation CLINVAR The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype? 9158144 1997
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype? 9158144 1997
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 CausalMutation CLINVAR Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies. 7603790 1995
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies. 7603790 1995
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Four compound heterozygote individuals from two unrelated families with A985G on one allele and a novel G to A mutation at nucleotide 583 (G583A) as the second mutant allele presented with MCAD deficiency in the first week of life. 7929823 1994
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Disease-causing mutations in exon 11 of the medium-chain acyl-CoA dehydrogenase gene. 8198141 1994
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 CausalMutation CLINVAR Four compound heterozygote individuals from two unrelated families with A985G on one allele and a novel G to A mutation at nucleotide 583 (G583A) as the second mutant allele presented with MCAD deficiency in the first week of life. 7929823 1994
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation BEFREE This novel mutation, G583A, is associated with severe MCAD deficiency causing hypoglycemia or sudden, unexpected neonatal death. 7929823 1994
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation CLINVAR Four compound heterozygote individuals from two unrelated families with A985G on one allele and a novel G to A mutation at nucleotide 583 (G583A) as the second mutant allele presented with MCAD deficiency in the first week of life. 7929823 1994
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene. 1363805 1992
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Frequency of the G985 MCAD mutation in the general population. 1671131 1991
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Molecular survey of a prevalent mutation, 985A-to-G transition, and identification of five infrequent mutations in the medium-chain Acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiency. 1684086 1991
Medium-chain acyl-coenzyme A dehydrogenase deficiency
0.810 GeneticVariation UNIPROT Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli. 1902818 1991