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FOXN1

forkhead box N1

gene with protein productOMIM: 6008383 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)3
Severe combined immunodeficiency due to FOXN1 deficiencyORPHA:169095
→
T-cell immunodeficiency with thymic aplasiaORPHA:83471
→
Combined immunodeficiency due to FOXN1 haploinsufficiencyORPHA:676039
→
Данные: Orphadata (CC-BY-4.0)