NDUFA7

NADH:ubiquinone oxidoreductase subunit A7
OMIM: 602139, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red NDUFA7 in Mendeliome


Version 1.2374

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Optic atrophy, MONDO:0003608, NDUFA7-related

Red NDUFA7 in Optic Atrophy


Level 2: Ophthalmological disorders
Version 1.45

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Other
    Phenotypes
    • Optic atrophy, MONDO:0003608, NDUFA7-related