Disease table of ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS OMIM ID: 300673

Gene-disease associations table

Gene	Associated with ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
MECP2	OMIM	HGNC link	Xq28	6	300673, PS309510, PS209850, 312750, 143465, 105830