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BabyScreen+ newborn screening v1.114 | AKT3 | Tommy Li Added phenotypes Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome for gene: AKT3 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BabyScreen+ newborn screening v0.0 | AKT3 |
Zornitza Stark gene: AKT3 was added gene: AKT3 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: AKT3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: AKT3 were set to Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome |