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| Genomic newborn screening: BabyScreen+ v2.0 | ALG11 | Gene migrated from ENSG00000253710 to ENSG00000253710 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | ALG11 |
Zornitza Stark gene: ALG11 was added gene: ALG11 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: ALG11 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ALG11 were set to Congenital disorder of glycosylation type 1P |
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