FOXN1, forkhead box N1, 8456

N. diseases: 60; N. variants: 5
Disease: Congenital alopecia X-linked ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3495530
Disease: Congenital alopecia X-linked
Congenital alopecia X-linked 		0.010 GeneticVariation disease BEFREE Alterations of the FOXN1 gene in both mice and humans result in a severe combined immunodeficiency caused by an intrinsic defect of the thymus associated with congenital alopecia (Nude/severe combined immunodeficiency phenotype). 18339010 2008