idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes
Go to external page http://purl.obolibrary.org/obo/MONDO_0015654
This is just here as a test because I lose it
Term information
database
cross reference
- Orphanet:166475
- UMLS:CN200064
Subsets
ordo_group_of_disorders
exactMatch
http://linkedlifedata.com/resource/umls/id/CN200064
http://www.orpha.net/ORDO/Orphanet_166475