| Multiple Acyl Coenzyme A Dehydrogenase Deficiency |
C0268596 |
ETFA
|
Causal
Pathogenic evidence from ClinVar
|
1430199, 1882842, 9334218, 12815589, 15159392, 16510302, 18289905, 20023066, 20736750, 23785301, 25929793, 26409463 |
ClinVar |
|
ETFB
|
Causal
Pathogenic evidence from ClinVar
|
7912128, 8504797, 12706375, 12815589, 15159392, 16510302, 18289905, 25416781, 25929793, 27081516 |
ClinVar |
|
ETFDH
|
Causal
Pathogenic evidence from ClinVar
|
2989828, 3620453, 12359134, 12815589, 15669683, 16510302, 16527485, 17412732, 17584774, 18289905, 19249206, 19265687, 20020044, 20370797, 21088898, 21907580, 22013910, 22580358, 22611163, 22664151, 23628458, 23727839, 23785301, 24123825, 24190796, 24357026, 24522293, 25929793, 26403312, 27000805, 27038534, 27270537, 27935074, 29249369 |
ClinVar |
|
FLAD1
|
Causal
Pathogenic evidence from ClinVar
|
27259049 |
ClinVar |
| Multiple acyl-CoA dehydrogenase deficiency, mild type |
394532 |
ETFA
|
Causal
Pathogenic evidence from ClinVar
|
- |
ClinVar |
|
ETFB
|
Causal
Pathogenic evidence from ClinVar
|
- |
ClinVar |
|
ETFDH
|
Causal
Pathogenic evidence from ClinVar
|
- |
ClinVar |
|
FLAD1
|
Causal
Pathogenic evidence from ClinVar
|
- |
ClinVar |
|
SLC25A32
|
Unknown
Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations
|
- |
- |
| Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type |
394529 |
ETFA
|
Causal
Pathogenic evidence from ClinVar
|
- |
ClinVar |
|
ETFB
|
Causal
Pathogenic evidence from ClinVar
|
- |
ClinVar |
|
ETFDH
|
Causal
Pathogenic evidence from ClinVar
|
- |
ClinVar |
|
FLAD1
|
Causal
Pathogenic evidence from ClinVar
|
- |
ClinVar |
