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| Vitamin metabolism disorders v2.0 | NMNAT1 | Gene migrated from ENSG00000173614 to ENSG00000173614 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v1.2 | NMNAT1 |
Bryony Thompson gene: NMNAT1 was added gene: NMNAT1 was added to Vitamin metabolism disorders. Sources: Expert Review Green Mode of inheritance for gene: NMNAT1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: NMNAT1 were set to 32533184 Phenotypes for gene: NMNAT1 were set to Disorders of niacin and NAD metabolism; Leber congenital amaurosis 9 MONDO:0012056 |
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