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| Additional findings_Paediatric v1.0 | MYO1F | Gene migrated from ENSG00000142347 to ENSG00000142347 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | MYO1F |
Zornitza Stark gene: MYO1F was added gene: MYO1F was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: MYO1F was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: MYO1F were set to Sensorineural hearing loss |
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