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| Leukodystrophy - paediatric v0.10 | COQ9 |
Bryony Thompson gene: COQ9 was added gene: COQ9 was added to Leukodystrophy - paediatric_RMH. Sources: Expert list Mode of inheritance for gene: COQ9 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: COQ9 were set to Coenzyme Q10 deficiency, primary, 5 614654 Review for gene: COQ9 was set to RED Added comment: White matter changes are not reported as a prominent feature of the condition. Sources: Expert list |
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