Disease table of FRAGILE X MENTAL RETARDATION SYNDROME OMIM ID: 300624

Gene-disease associations table

Gene	Associated with FRAGILE X MENTAL RETARDATION SYNDROME in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
FMR1	ClinVar, OMIM, HUMSAVAR	HGNC link	Xq27.3	3	300624, 300623, 311360