PCDHGC4

protocadherin gamma subfamily C, 4
OMIM: 606305, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green PCDHGC4 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with poor growth and skeletal anomalies, MIM# 619880

Green PCDHGC4 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 Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with poor growth and skeletal anomalies, MIM# 619880

    Green PCDHGC4 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with poor growth and skeletal anomalies, MIM# 619880

    Green PCDHGC4 in Growth failure


    Version 1.76

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Neurodevelopmental disorder with poor growth and skeletal anomalies, MIM# 619880