forkhead box F2
OMIM: 603250, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red FOXF2 in Familial cerebral small vessel disease

Level 3: Arteriopathies
Level 2: Cardiovascular disorders
Version 1.17

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
  • Literature
  • Small vessel stroke
Amber FOXF2 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.41
Latest signed off version: v4.39 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    • Expert Review Amber
    • Literature
    • profound sensorineural hearing loss (SNHL)
    • cochlea malformations
    • incomplete partition type I anomaly of the cochlea