FOXF2

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 1.10

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
Phenotypes
  • Small vessel stroke

Amber FOXF2 in Hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 2.159
Latest signed off version: v2.158 (29 Jun 2021)

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