MT-CO3

mitochondrially encoded cytochrome c oxidase III
OMIM: 516050
PanelMode of inheritanceDetails
2 panels
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R98
Signed-off version 2.3
MITOCHONDRIAL
Phenotypes
LEBER OPTIC ATROPHY, SEIZURES AND LACTIC ACIDOSIS, MITOCHONDRIAL COMPLEX IV DEFICIENCY
Component of the following Super Panels:
  • - White matter disorders - childhood onset
Signed-off version 2.4
MITOCHONDRIAL
Phenotypes