MICU2

mitochondrial calcium uptake 2
OMIM: 610632, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red MICU2 in Mitochondrial disorders


Level 2: Mitochondrial
Version 9.41
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • review Not set
    Sources
    • Expert list
    Phenotypes
    • severe cognitive impairment and spasticity