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| Vitamin metabolism disorders v2.0 | MMAA | Gene migrated from ENSG00000151611 to ENSG00000151611 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v1.2 | MMAA |
Bryony Thompson gene: MMAA was added gene: MMAA was added to Vitamin metabolism disorders. Sources: Expert Review Green Mode of inheritance for gene: MMAA was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MMAA were set to 12438653; 15523652 Phenotypes for gene: MMAA were set to Disorders of cobalamin metabolism; methylmalonic aciduria, cblA type MONDO:0009613 |
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