Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024

Preferred Name	Rare genetic epilepsy
Synonyms
ID	http://www.orpha.net/ORDO/Orphanet_183512
expertlink	https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=183512
hasDbXref	UMLS:C5680564
label	Rare genetic epilepsy
notation	ORPHA:183512 Category
prefixIRI	ORDO:Orphanet_183512
prefLabel	Rare genetic epilepsy
subClassOf	http://www.orpha.net/ORDO/Orphanet_557492 http://www.orpha.net/ORDO/Orphanet_71859

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://www.orpha.net/ORDO/Orphanet_183512	CCONT	SAME_URI
http://www.orpha.net/ORDO/Orphanet_183512	EFO	SAME_URI
http://www.orpha.net/ORDO/Orphanet_183512	EFO	SAME_URI
http://www.limics.org/hrdo/rdfns#pat_id_18257	HRDO	LOOM
http://www.orpha.net/ORDO/Orphanet_183512	CCONT	LOOM
http://www.orpha.net/ORDO/Orphanet_183512	EFO	LOOM
http://www.orpha.net/ORDO/Orphanet_183512	EFO	LOOM