ZDHHC15

zinc finger DHHC-type containing 15
OMIM: 300576, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red ZDHHC15 in DDG2P


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

Component of the following Super Panels:

  • Paediatric disorders
  • review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • MENTAL RETARDATION X-LINKED TYPE 91 300577
    Red ZDHHC15 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 X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Red
    • Emory Genetics Laboratory
    Phenotypes
    • cerebral palsy
    • intellectual disability
    • autism spectrum disorder
    • epilepsy