IRF6, interferon regulatory factor 6, 3664

N. diseases: 233; N. variants: 43
Disease: Myopathy, Actin, Congenital, with Excess of Thin Myofilaments ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1834339
Disease: Myopathy, Actin, Congenital, with Excess of Thin Myofilaments
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments 		0.200 Biomarker disease MGD Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse. 20196077 2010