| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Likely inborn error of metabolism - targeted testing not possible v0.4 | COG2 |
Ellen McDonagh gene: COG2 was added gene: COG2 was added to Inborn errors of metabolism. Sources: Expert Review Red Mode of inheritance for gene: COG2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: COG2 were set to 11980916; 24784932 Phenotypes for gene: COG2 were set to ?Congenital disorder of glycosylation, type IIq, 617395 |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||