SNOMED Terminos Clinicos

Last uploaded: August 28, 2024

Preferred Name	enfermedad de von Willebrand hereditaria tipo 2B
Synonyms	enfermedad de von Willebrand hereditaria tipo 2B (trastorno)
ID	http://purl.bioontology.org/ontology/SCTSPA/359717002
Active	1
altLabel	enfermedad de von Willebrand hereditaria tipo 2B (trastorno)
CASE SIGNIFICANCE ID	900000000000017005
cui	C1282971
DEFINITION STATUS ID	900000000000074008
Effective time	20020131
Has interpretation	http://purl.bioontology.org/ontology/SCTSPA/263654008
interprets	http://purl.bioontology.org/ontology/SCTSPA/74848003
Module ID	450829007
notation	359717002
prefLabel	359717002
Subset member	450828004~ACCEPTABILITYID~900000000000548007
tui	T047
Type ID	900000000000003001 900000000000013009
subClassOf	http://purl.bioontology.org/ontology/SCTSPA/128107007 http://purl.bioontology.org/ontology/SCTSPA/11164009

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/SNMI/DC-64140	SNMI	CUI
http://purl.bioontology.org/ontology/MESH/D056728	MESH	CUI
http://purl.bioontology.org/ontology/OMIM/613160	OMIM	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/359717002	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/MSHFRE/D056728	MSHFRE	CUI
http://purl.bioontology.org/ontology/ICD10CM/D68.021	ICD10CM	CUI
http://purl.bioontology.org/ontology/OMIM/613554	OMIM	CUI