TOMM70

translocase of outer mitochondrial membrane 70
OMIM: 606081, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber TOMM70 in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Severe anaemia, lactic acidosis, developmental delay
  • White matter abnormalities, developmental delay, regression, movement disorder

Amber TOMM70 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.927

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Severe anaemia
    • Lactic acidosis
    • Developmental delay

    Amber TOMM70 in Leukodystrophy - paediatric


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.308

    Component of the following Super Panels:

  • Leukodystrophy_Superpanel
  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • White matter abnormalities
    • Developmental delay
    • Regression
    • Movement disorder