MMS19

MMS19 homolog, cytosolic iron-sulfur assembly component
OMIM: 614777, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red MMS19 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodegenerative disease, MONDO:0005559, MMS19-related

Red MMS19 in Muscular dystrophy and myopathy_Paediatric


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Myopathy Superpanel
  • Neuromuscular Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Neurodegenerative disease, MONDO:0005559, MMS19-related

    Red MMS19 in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.33

    Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Neurodegenerative disease, MONDO:0005559, MMS19-related

    Red MMS19 in Regression


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.556

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Neurodegenerative disease, MONDO:0005559, MMS19-related