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| Genomic newborn screening: BabyScreen+ v2.0 | BPGM | Gene migrated from ENSG00000172331 to ENSG00000172331 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | BPGM |
Zornitza Stark gene: BPGM was added gene: BPGM was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: BPGM was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: BPGM were set to Erythrocytosis due to bisphosphoglycerate mutase deficiency |
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