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| Vitamin metabolism disorders v2.0 | ETFDH | Gene migrated from ENSG00000171503 to ENSG00000171503 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v1.2 | ETFDH |
Bryony Thompson gene: ETFDH was added gene: ETFDH was added to Vitamin metabolism disorders. Sources: Expert Review Green Mode of inheritance for gene: ETFDH was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ETFDH were set to 17412732, 27038534, 19249206, 15710863, 32804429 Phenotypes for gene: ETFDH were set to multiple acyl-CoA dehydrogenase deficiency MONDO:0009282; Disorders of mitochondrial fatty acid oxidation |
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