FOXD3

forkhead box D3
OMIM: 611539, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red FOXD3 in Eye Anterior Segment Abnormalities


Level 2: Ophthalmological disorders
Version 1.17

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • ClinGen
Phenotypes
  • Aniridia, MONDO:0019172
Tags
  • disputed

Red FOXD3 in Mendeliome


Version 1.3795

2 reviews Unknown
Sources
  • Expert Review Red
  • ClinGen
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Autoimmune disease, susceptibility to, 1 MONDO:0011919
  • Aniridia, MONDO:0019172
Tags
  • disputed