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| Genomic newborn screening: BabyScreen+ v2.0 | GFER | Gene migrated from ENSG00000127554 to ENSG00000127554 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | GFER |
Zornitza Stark gene: GFER was added gene: GFER was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: GFER was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: GFER were set to Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay |
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