FOXL2, forkhead box L2, 668

N. diseases: 137; N. variants: 102
Disease: Bpes, Type I, Autosomal Recessive ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1970106
Disease: Bpes, Type I, Autosomal Recessive
Bpes, Type I, Autosomal Recessive 		0.300 Biomarker disease CTD_human Blepharophimosis and bilateral Duane syndrome associated with a FOXL2 mutation. 16283882 2005