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 7.6
Latest signed off version: v7.0 (30 Apr 2025)

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


Level 2: Ophthalmology
Version 4.37
Latest signed off version: v4.0 (7 Aug 2024)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Anterior segment dysgenesis
  • Peters anomaly
  • aniridia
Tags
  • Q3_25_expert_review
  • disputed
  • Q3_25_demote_red