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| Genomic newborn screening: BabyScreen+ v2.0 | PEX11B | Gene migrated from ENSG00000131779 to ENSG00000131779 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | PEX11B |
Zornitza Stark gene: PEX11B was added gene: PEX11B was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: PEX11B was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: PEX11B were set to Peroxisome biogenesis disorder |
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