FBXO8

F-box protein 8
OMIM: 605649, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red FBXO8 in Intellectual disability


Level 2: Developmental disorders
Version 9.288
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review Not set
    Sources
    • Expert Review Red
    • Expert Review Red
    Phenotypes
    • moderate developmental delay