KDM4B

lysine demethylase 4B
OMIM: 609765, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green KDM4B in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Intellectual developmental disorder, autosomal dominant 65, MIM# 619320
  • Global developmental delay, intellectual disability and neuroanatomical defects

Green KDM4B in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Intellectual developmental disorder, autosomal dominant 65, MIM# 619320
    • Global developmental delay, intellectual disability and neuroanatomical defects

    Green KDM4B in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Intellectual developmental disorder, autosomal dominant 65, MIM# 619320
    • Global developmental delay, intellectual disability and neuroanatomical defects