C12orf66

chromosome 12 open reading frame 66
OMIM: 617420, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green C12orf66 in Mendeliome


Version 1.2374

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Other
Phenotypes
  • Intellectual developmental disorder, autosomal recessive 83, MIM# 621100
Tags
  • new gene name

Green C12orf66 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.119

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Intellectual developmental disorder, autosomal recessive 83, MIM# 621100
    Tags
    • new gene name

    Green C12orf66 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.83

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Other
    Phenotypes
    • Intellectual developmental disorder, autosomal recessive 83, MIM# 621100
    Tags
    • new gene name