ZNF526

zinc finger protein 526
OMIM: 614387, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green ZNF526 in Cataract


Level 2: Ophthalmological disorders
Version 0.373

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Dentici-Novelli neurodevelopmental syndrome, MIM# 619877

Green ZNF526 in Mendeliome


Version 1.2374

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Dentici-Novelli neurodevelopmental syndrome, MIM# 619877

Green ZNF526 in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.301

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Dentici-Novelli neurodevelopmental syndrome, MIM# 619877

Green ZNF526 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
    • Dentici-Novelli neurodevelopmental syndrome, MIM# 619877

    Green ZNF526 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
    • Literature
    Phenotypes
    • Dentici-Novelli neurodevelopmental syndrome, MIM# 619877

    Green ZNF526 in Dystonia - complex


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.272

    Component of the following Super Panels:

  • Dystonia_Superpanel
  • Progressive Neurological Conditions
  • Tremors_Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Dentici-Novelli neurodevelopmental syndrome, MIM# 619877

    Green ZNF526 in Fetal anomalies


    Version 1.314

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Dentici-Novelli neurodevelopmental syndrome, MIM# 619877