Disease core ontology applied to Rare Diseases

Last uploaded: February 7, 2014

Preferred Name	Familial or sporadic hemiplegic migraine
Synonyms
ID	http://www.limics.org/hrdo/rdfns#pat_id_1031
ageOfDeath	Normal
ageOfOnset	Childhood
id_Medline	http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=Search&Term=familial+hemiplegic+migraine%5Btw%5D+OR+%28%22classic+migraine%22%5BMeSH+Terms%5D+AND+hemiplegic%5Btw%5D%29
id_MIM	141500 602481 607516 609634
id_OMS	G43.1
id_Orpha	569
inheritance	Autosomal dominant
patType	disease
prefixIRI	hrdo:pat_id_1031
prefLabel	Familial or sporadic hemiplegic migraine
prevalence	1-5 / 10 000
subClassOf	http://www.limics.org/hrdo/rdfns#typ_id_11

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://www.orpha.net/ORDO/Orphanet_569	ORDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0018925	MONDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0018925	CCONT	LOOM
http://purl.obolibrary.org/obo/MONDO_0018925	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0018925	DOVES	LOOM
http://www.orpha.net/ORDO/Orphanet_569	ORDO	LOOM