377794 group of disorders
71859 Rare genetic neurological disorder
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183512 Rare genetic epilepsy
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166463 Epilepsy syndrome
4
166466 Neurocutaneous syndrome with epilepsy
166472 Monogenic disease with epilepsy
4
166475 Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes
1
166478 Cerebral malformation with epilepsy
3
166487 Cerebral diseases of vascular origin with epilepsy