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| Hydrops fetalis v0.115 | AKT3 | Zornitza Stark Marked gene: AKT3 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.115 | AKT3 | Zornitza Stark Gene: akt3 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.115 | AKT3 |
Zornitza Stark gene: AKT3 was added gene: AKT3 was added to Hydrops fetalis. Sources: Expert list Mode of inheritance for gene: AKT3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: AKT3 were set to 23754335 Phenotypes for gene: AKT3 were set to Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2, MIM# 615937 Review for gene: AKT3 was set to RED Added comment: Single case report of MCAP with fetal hydrops presentation, PIK3CA variant identified. Sources: Expert list |
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