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| Genomic newborn screening: BabyScreen+ v2.0 | MYO5A | Gene migrated from ENSG00000197535 to ENSG00000197535 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | MYO5A |
Zornitza Stark gene: MYO5A was added gene: MYO5A was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: MYO5A was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: MYO5A were set to Griscelli syndrome |
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