Table 1. Twenty three MeSH headings of RE subtypes.

NO.	MeSH heading	Unique ID	NO.	MeSH heading	Unique ID
1	Alexander Disease	D038261	13	Malformations of Cortical Development	D054220
2	Anti-N-Methyl-D-Aspartate Receptor Encephalitis	D060426	14	MELAS Syndrome	D017241
3	Classical Lissencephalies and Subcortical Band Heterotopias	D054221	15	MERRF Syndrome	D017243
4	Epilepsies, Myoclonic	D004831	16	Mitochondrial Encephalomyopathies	D017237
5	Epilepsy, Absence	D004832	17	Myoclonic Epilepsies, Progressive	D020191
6	Epilepsy, Frontal Lobe	D017034	18	Myoclonic Epilepsy, Juvenile	D020190
7	Epilepsy, Temporal Lobe	D004833	19	Neuronal Ceroid-Lipofuscinoses	D009472
8	Fragile X Syndrome	D005600	20	Rett Syndrome	D015518
9	Lafora Disease	D020192	21	Spasms, Infantile	D013036
10	Landau-Kleffner Syndrome	D018887	22	Tuberous Sclerosis	D014402
11	Leigh Disease	D007888	23	Unverricht-Lundborg Syndrome	D020194
12	Lissencephaly	D054082