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| Vitamin metabolism disorders v2.0 | BCO1 | Gene migrated from ENSG00000135697 to ENSG00000135697 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v1.2 | BCO1 |
Bryony Thompson gene: BCO1 was added gene: BCO1 was added to Vitamin metabolism disorders. Sources: Expert Review Red Mode of inheritance for gene: BCO1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: BCO1 were set to 17951468 Phenotypes for gene: BCO1 were set to Other disorders of vitamin metabolism; hereditary hypercarotenemia and vitamin A deficiency MONDO:0007272 |
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