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 3.1
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 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
T-B+ SCID, T-B+ SCID, congenital alopecia, nail dystrophy, 601705, T-cell immunodeficiency, congenital alopecia, and nail dystrophy, Nude severe combined immunodeficiency, Severe infections, abnormal thymic epithelium, immunodeficiency, congenital alopecia, nail dystrophy, neural tube defect, Combined immunodeficiencies with associated or syndromic features