ZFX

zinc finger protein, X-linked
OMIM: 314980, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber ZFX in Intellectual disability - microarray and sequencing

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.550
Latest signed off version: v5.0 (22 Mar 2023)

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 Amber
    Phenotypes
    • Intellectual developmental disorder, X-linked syndromic 37, OMIM:301118
    Tags
    • Q1_24_promote_green
    • Q1_24_NHS_review