FOXD3

forkhead box D3
OMIM: 611539, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red FOXD3 in Glaucoma (developmental)

Level 3: Anterior segment abnormalities
Level 2: Ophthalmological disorders
Version 1.47

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • NHS GMS
  • GDL Glaucoma panel
Phenotypes
  • Anterior segment dysgenesis
  • Peters anomaly
  • aniridia
Red FOXD3 in Bilateral congenital or childhood onset cataracts


Level 2: Ophthalmology
Version 8.1
Latest signed off version: v8.0 (6 May 2026)

review Unknown
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Anterior segment dysgenesis, Peter’s anomaly
Red FOXD3 in Structural eye disease


Level 2: Ophthalmology
Version 5.6
Latest signed off version: v5.0 (6 May 2026)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • NHS GMS
Phenotypes
  • Anterior segment dysgenesis
  • Peters anomaly
  • aniridia
Tags
  • disputed