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FOXN1

forkhead box N1

HCNC Approved Symbol
FOXN1 (HGNC:12765)
Genomic Coordinates
17:28,506,348 - 28,538,900 (17q11.2)
Synonyms
FKHL20, WHN, RONU
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
601705AR
T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant
618806AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the FOXN1 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results