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| Liver Failure_Paediatric v0.62 | COQ2 | Zornitza Stark Marked gene: COQ2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Liver Failure_Paediatric v0.62 | COQ2 | Zornitza Stark Gene: coq2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Liver Failure_Paediatric v0.62 | COQ2 |
Zornitza Stark gene: COQ2 was added gene: COQ2 was added to Liver Failure_Paediatric. Sources: Expert list Mode of inheritance for gene: COQ2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: COQ2 were set to 17332895 Phenotypes for gene: COQ2 were set to Coenzyme Q10 deficiency, primary, 1, MIM#607426 Review for gene: COQ2 was set to RED Added comment: Manifestations of this disorder are principally encephalomyopathic and renal, however at least one report of liver failure. Sources: Expert list |
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