FOXN1

PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ALOPECIA AND T-CELL IMMUNODEFICIENCY 601705
R-numbers: R15
Signed-off version 2.1
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