PIGF

phosphatidylinositol glycan anchor biosynthesis class F
OMIM: 600153, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red PIGF in Congenital Disorders of Glycosylation


Level 2: Metabolic disorders
Version 1.44

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome, MIM# 619356

    Red PIGF in Mendeliome


    Version 1.1891

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome, MIM# 619356

    Red PIGF 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
    • Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome, MIM#619356

    Red PIGF in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome, MIM# 619356