Disease table of RETT SYNDROME OMIM ID: 312750

Gene-disease associations table

Gene	Associated with RETT SYNDROME in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
MECP2	ClinVar, OMIM, HUMSAVAR	HGNC link	Xq28	6	300673, PS309510, PS209850, 312750, 143465, 105830