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| Genomic newborn screening: BabyScreen+ v2.0 | IFT122 | Gene migrated from ENSG00000163913 to ENSG00000163913 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | IFT122 |
Zornitza Stark gene: IFT122 was added gene: IFT122 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: IFT122 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: IFT122 were set to Cranioectodermal dysplasia |
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