Disease core ontology applied to Rare Diseases

Last uploaded: February 7, 2014

Preferred Name	Von Willebrand disease type 2N
Synonyms
ID	http://www.limics.org/hrdo/rdfns#pat_id_17616
id_Medline	neant
id_MIM	613554
id_OMS	D68.0
id_Orpha	166093
id_SNOMEDCT	359732009
id_UMLS	C1282975
inheritance	Autosomal recessive
patType	clinical subtype
prefixIRI	hrdo:pat_id_17616
prefLabel	Von Willebrand disease type 2N
prevalence	Unknown
subClassOf	http://www.limics.org/hrdo/rdfns#typ_id_2

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0015631	MONDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0015631	CCONT	LOOM
http://purl.obolibrary.org/obo/MONDO_0015631	DOVES	LOOM
http://purl.obolibrary.org/obo/MONDO_0015631	EFO	LOOM
http://www.orpha.net/ORDO/Orphanet_166093	ORDO	LOOM
http://purl.bioontology.org/ontology/ICD10CM/D68.023	ICD10CM	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C131689	NCIT	LOOM
http://purl.obolibrary.org/obo/NCIT_C131689	BERO	LOOM