FXR1, FMR1 autosomal homolog 1, 8087

N. diseases: 53; N. variants: 7
Disease: Congenital Heart Defects ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		0.010 AlteredExpression group BEFREE FXR1P is expressed throughout the body and important for normal muscle development, and its absence causes cardiac abnormality. 27357083 2016