MICOS13

mitochondrial contact site and cristae organizing system subunit 13
OMIM: 616658, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green MICOS13 in Mendeliome


Version 2.49

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Combined oxidative phosphorylation deficiency 37, MIM# 618329
Tags
  • new gene name

Green MICOS13 in Mitochondrial disease


Level 2: Metabolic disorders
Version 2.0

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Combined oxidative phosphorylation deficiency 37, MIM# 618329
    Tags
    • new gene name