Disease core ontology applied to Rare Diseases

Last uploaded: February 7, 2014

Preferred Name	Von Willebrand disease type 2B
Synonyms
ID	http://www.limics.org/hrdo/rdfns#pat_id_17614
id_Medline	neant
id_MIM	613554
id_OMS	D68.0
id_Orpha	166087
id_SNOMEDCT	19520006 359717002 359721009
id_UMLS	C1282971
inheritance	Autosomal dominant
patType	clinical subtype
prefixIRI	hrdo:pat_id_17614
prefLabel	Von Willebrand disease type 2B
prevalence	Unknown
subClassOf	http://www.limics.org/hrdo/rdfns#typ_id_2

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0015629	MONDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0015629	CCONT	LOOM
http://purl.obolibrary.org/obo/MONDO_0015629	HSPO	LOOM
http://purl.obolibrary.org/obo/MONDO_0015629	DOVES	LOOM
http://purl.obolibrary.org/obo/MONDO_0015629	EFO	LOOM
http://www.orpha.net/ORDO/Orphanet_166087	ORDO	LOOM
http://id.nlm.nih.gov/mesh/D056728	MDM	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C131687	NCIT	LOOM
http://purl.obolibrary.org/obo/NCIT_C131687	BERO	LOOM
http://purl.bioontology.org/ontology/ICD10CM/D68.021	ICD10CM	LOOM