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| Genomic newborn screening: BabyScreen+ v2.0 | COG7 | Gene migrated from ENSG00000168434 to ENSG00000168434 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | COG7 |
Zornitza Stark gene: COG7 was added gene: COG7 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: COG7 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: COG7 were set to Congenital disorder of glycosylation, type IIe |
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