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| Vitamin metabolism disorders v2.0 | EPHX1 | Gene migrated from ENSG00000143819 to ENSG00000143819 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v1.2 | EPHX1 |
Bryony Thompson gene: EPHX1 was added gene: EPHX1 was added to Vitamin metabolism disorders. Sources: Expert Review Red Mode of inheritance for gene: EPHX1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: EPHX1 were set to 34342583 Phenotypes for gene: EPHX1 were set to Familial hypercholanemia MONDO:0011905; Other disorders of vitamin metabolism |
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