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| Additional findings_Paediatric v1.0 | COG4 | Gene migrated from ENSG00000103051 to ENSG00000103051 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | COG4 |
Zornitza Stark gene: COG4 was added gene: COG4 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: COG4 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: COG4 were set to Congenital disorder of glycosylation, type IIj |
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