FOXD3

forkhead box D3
OMIM: 611539, Gene2Phenotype

3 panels

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

Level 3: Anterior segment abnormalities
Level 2: Ophthalmological disorders
Version 1.45

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

Level 3: Anterior segment abnormalities
Level 2: Ophthalmological disorders
Version 4.8
Latest signed off version: v4.0 (22 Mar 2023)

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


Version 3.74
Latest signed off version: v3.0 (22 Mar 2023)

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