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Hydrops fetalis v0.147 | PIK3R2 |
Zornitza Stark gene: PIK3R2 was added gene: PIK3R2 was added to Hydrops fetalis. Sources: Expert list Mode of inheritance for gene: PIK3R2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: PIK3R2 were set to 23754335 Phenotypes for gene: PIK3R2 were set to Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2, MIM# 615937 Review for gene: PIK3R2 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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Hydrops fetalis v0.146 | PIK3CA | Zornitza Stark Marked gene: PIK3CA as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Hydrops fetalis v0.146 | PIK3CA | Zornitza Stark Gene: pik3ca has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Hydrops fetalis v0.146 | PIK3CA |
Zornitza Stark gene: PIK3CA was added gene: PIK3CA was added to Hydrops fetalis. Sources: Expert list Mode of inheritance for gene: PIK3CA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: PIK3CA were set to 23754335 Phenotypes for gene: PIK3CA were set to Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2, MIM# 615937 Review for gene: PIK3CA 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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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 |