MICU2

mitochondrial calcium uptake 2
OMIM: 610632, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red MICU2 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 Red
    • NHS GMS
    Phenotypes
    • cognitive impairment
    • spasticity
    • white matter involvement