| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Vitamin metabolism disorders v0.5 | MMAB | Bryony Thompson Marked gene: MMAB as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v0.5 | MMAB | Bryony Thompson Gene: mmab has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v0.5 | MMAB | Bryony Thompson Classified gene: MMAB as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v0.5 | MMAB | Bryony Thompson Gene: mmab has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v0.4 | MMAB |
Bryony Thompson gene: MMAB was added gene: MMAB was added to Inherited vitamin B12 or cobalamin deficiency. Sources: Literature Mode of inheritance for gene: MMAB was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MMAB were set to 12471062; 20556797; 35712814; 24813872 Phenotypes for gene: MMAB were set to methylmalonic aciduria, cblB type MONDO:0009614 Review for gene: MMAB was set to GREEN gene: MMAB was marked as current diagnostic Added comment: Well-established gene-disease association. Inborn error of cobalamin metabolism. Sources: Literature |
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