FOXI3

forkhead box I3
OMIM: 612351, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green FOXI3 in Mandibulofacial Acrofacial dysostosis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.22

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Craniofacial microsomia 2, MIM# 620444

Green FOXI3 in Mendeliome


Version 1.4865

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Craniofacial microsomia 2, MIM# 620444

Amber FOXI3 in Combined Immunodeficiency


Level 2: Immunological disorders
Version 1.147

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • thymic dysplasia MONDO:0004195