Genomics England
GMS Panels
Panels
Genes and Entities

COQ7

coenzyme Q7, hydroxylase
OMIM: 601683
PanelMode of inheritanceDetails
3 panels
Green
in Inborn errors of metabolism
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R98
Signed-off version 3.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Coenzyme Q10 deficiency, primary, 8 616733
Green
in Mitochondrial disorders
Component of the following Super Panels:
  • - White matter disorders - childhood onset
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Coenzyme Q10 deficiency, primary, 8 616733, complex multisystem presentation
Green
in Possible mitochondrial disorder - nuclear genes
R-numbers: R63
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
?Coenzyme Q10 deficiency, primary, 8 616733