View all diseases

Legend

Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

1 entry on 1 page. Showing entry 1.

ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes
00019	RTT	RETT SYNDROME	312750	0	0	MECP2