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| Genomic newborn screening: BabyScreen+ v2.0 | MYO1C | Gene migrated from ENSG00000197879 to ENSG00000197879 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | MYO1C |
Zornitza Stark gene: MYO1C was added gene: MYO1C was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: MYO1C was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: MYO1C were set to Sensorineural hearing loss |
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