C9orf3

chromosome 9 open reading frame 3
ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green C9orf3 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.49

Component of the following Super Panels:

  • Movement Disorders Superpanel
  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions
  • 2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Dystonia 31, MIM# 619565
    • Childhood/Adolescence onset generalised dystonia
    • Dystonia parkinsonism
    • Zech-Boesch Syndrome
    Tags
    • new gene name

    Green C9orf3 in Mendeliome


    Version 1.4220

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Dystonia 31, MIM# 619565

    Green C9orf3 in Dystonia and Chorea


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.337

    Component of the following Super Panels:

  • Movement Disorders Superpanel
  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    • Expert Review Green
    • Expert Review Green
    • Literature
    Phenotypes
    • Dystonia 31, MIM# 619565
    Tags
    • new gene name