Activity
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| Likely inborn error of metabolism v8.60 | SLC46A1 | Arina Puzriakova Phenotypes for gene: SLC46A1 were changed from Folate malabsorption, hereditary; Hereditary folate malabsorption (Disorders of folate metabolism and transport) to Folate malabsorption, hereditary, OMIM:229050; Hereditary folate malabsorption (Disorders of folate metabolism and transport) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Likely inborn error of metabolism v1.47 | SLC46A1 |
Ivone Leong Source NHS GMS was added to SLC46A1. Source London North GLH was added to SLC46A1. |
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| Likely inborn error of metabolism v0.4 | SLC46A1 |
Ellen McDonagh gene: SLC46A1 was added gene: SLC46A1 was added to Inborn errors of metabolism. Sources: Expert Review Green Mode of inheritance for gene: SLC46A1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SLC46A1 were set to 27604308 Phenotypes for gene: SLC46A1 were set to Folate malabsorption, hereditary; Hereditary folate malabsorption (Disorders of folate metabolism and transport) |
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