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| Hydrops fetalis v0.18 | COG6 | Zornitza Stark Marked gene: COG6 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.18 | COG6 | Zornitza Stark Gene: cog6 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.18 | COG6 |
Zornitza Stark gene: COG6 was added gene: COG6 was added to Hydrops fetalis_VCGS. Sources: Expert list Mode of inheritance for gene: COG6 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: COG6 were set to 31420886 Phenotypes for gene: COG6 were set to Congenital disorder of glycosylation, type Iil, MIM#614576 Review for gene: COG6 was set to RED Added comment: One family reported with hydrops, though hydrops is a presenting feature of a number of CDGs. Sources: Expert list |
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