1. Genes and Genomic Entities
  2. ZMYND8

ZMYND8

zinc finger MYND-type containing 8
OMIM: 615713, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green ZMYND8 in DDG2P


Version 4.3
Latest signed off version: v4.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • ZMYND8-related neurodevelopmental disorder
    Tags
    • gene-checked
    Green ZMYND8 in Intellectual disability

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 6.11
    Latest signed off version: v6.0 (1 May 2024)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Delayed speech and language development
    • Motor delay
    • Intellectual disability
    • Abnormality of cardiovascular system morphology
    • Hearing abnormality
    • Abnormality of vision
    • Abnormality of the face
    • Seizures
    Tags
    • gene-checked