Genomics England
GMS Panels
Panels
Genes and Entities

FOXN1

forkhead box N1
OMIM: 600838
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ALOPECIA AND T-CELL IMMUNODEFICIENCY 601705
Green
in Primary immunodeficiency or monogenic inflammatory bowel disease
R-numbers: R15
Signed-off version 7.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
T-cell immunodeficiency, congenital alopecia, and nail dystrophy, OMIM:601705 (AR), T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant, OMIM:618806 (AD), T-B+ SCID, Severe infections, abnormal thymic epithelium, immunodeficiency, congenital alopecia, nail dystrophy, neural tube defect, Combined immunodeficiencies with associated or syndromic features