COX19

COX19, cytochrome c oxidase assembly factor
OMIM: 610429, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red COX19 in Mitochondrial disorder with complex IV deficiency


Version 3.20
Latest signed off version: v3.0 (22 Mar 2023)

review Unknown
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • No OMIM phenotype
Red COX19 in Possible mitochondrial disorder - nuclear genes


Version 3.105
Latest signed off version: v3.0 (22 Mar 2023)

review Unknown
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • No OMIM phenotype
Red COX19 in Mitochondrial disorders

Level 3: Mitochondrial
Level 2: Metabolic disorders
Version 4.169
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • review Unknown
    Sources
    • Expert Review Red
    • NHS GMS
    Phenotypes
    • No OMIM phenotype