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| Additional findings_Paediatric v1.0 | PHKG2 | Gene migrated from ENSG00000156873 to ENSG00000156873 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | PHKG2 |
Zornitza Stark gene: PHKG2 was added gene: PHKG2 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: PHKG2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: PHKG2 were set to Phosphorylase kinase deficiency |
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