| | | Indel (frameshift variant +2 more) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (splice donor variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | See cases +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant +1 more) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Medium-chain acyl-coenzyme A dehydrogenase deficiency +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Medium-chain acyl-coenzyme A dehydrogenase deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | ACADM-related disorder +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (splice donor variant +1 more) | Medium-chain acyl-coenzyme A dehydrogenase deficiency +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Inborn genetic diseases +2 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | ACADM-related disorder +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Abnormal circulating lipid concentration +7 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | |
| | | Single nucleotide variant (missense variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | ACADM-related disorder +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | |
| | | Single nucleotide variant (stop lost) | Medium-chain acyl-coenzyme A dehydrogenase deficiency | |