FOXN1, forkhead box N1, 8456

N. diseases: 60; N. variants: 5
Disease: Congenital hypertrichosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2936812
Disease: Congenital hypertrichosis
Congenital hypertrichosis 		0.010 GeneticVariation disease BEFREE As far as we are aware, this is the first case of FOXN1 duplication associated with congenital hypertrichosis to be reported in the literature. 28297140 2017