1. Genes and Genomic Entities
  2. ZMYND8

ZMYND8

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

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber ZMYND8 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, ZMYND8-related
Green ZMYND8 in DDG2P


Version 6.424
Latest signed off version: v6.0 (30 Apr 2025)

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 2: Developmental disorders
    Version 9.285
    Latest signed off version: v9.0 (30 Apr 2025)

    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