TIMM22

translocase of inner mitochondrial membrane 22
OMIM: 607251, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber TIMM22 in Mendeliome


Version 1.3512

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • Mitochondrial disease, MONDO:0044970, TIMM22-related

Amber TIMM22 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.1085

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • 2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert Review Amber
    • NHS GMS
    • NHS GMS
    Phenotypes
    • Mitochondrial disease, MONDO:0044970, TIMM22-related