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| Hydrops fetalis v0.172 | ESCO2 | Zornitza Stark Marked gene: ESCO2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.172 | ESCO2 | Zornitza Stark Gene: esco2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.172 | ESCO2 |
Zornitza Stark gene: ESCO2 was added gene: ESCO2 was added to Hydrops fetalis. Sources: Expert list Mode of inheritance for gene: ESCO2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ESCO2 were set to 16547991 Phenotypes for gene: ESCO2 were set to Roberts syndrome, MIM# 268300 Review for gene: ESCO2 was set to RED Added comment: Single case report, diagnosis of Roberts syndrome not molecularly confirmed. Pregnancy complicated by T18 in other twin. Sources: Expert list |
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