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| BabyScreen+ newborn screening v1.114 | MYL2 | Tommy Li Added phenotypes Cardiomyopathy, familial hypertrophic, 10 for gene: MYL2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | MYL2 |
Zornitza Stark gene: MYL2 was added gene: MYL2 was added to gNBS. Sources: Expert Review Amber,BabySeq Category B gene Mode of inheritance for gene: MYL2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: MYL2 were set to Cardiomyopathy, familial hypertrophic, 10 |
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