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| Genomic newborn screening: BabyScreen+ v2.0 | SLC11A2 | Gene migrated from ENSG00000110911 to ENSG00000110911 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | SLC11A2 |
Zornitza Stark gene: SLC11A2 was added gene: SLC11A2 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: SLC11A2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SLC11A2 were set to Anemia, hypochromic microcytic |
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