SNOMED Terminos Clinicos

Last uploaded: August 28, 2024

Preferred Name	disfibrinogenemia hereditaria
Synonyms	disfibrinogenemia congénita disfibrinogenemia hereditaria (trastorno)
ID	http://purl.bioontology.org/ontology/SCTSPA/45366001
Active	1
altLabel	disfibrinogenemia congénita disfibrinogenemia hereditaria (trastorno)
CASE SIGNIFICANCE ID	900000000000020002 900000000000448009
cui	C0272350
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	45366001
Occurs in	http://purl.bioontology.org/ontology/SCTSPA/255399007
prefLabel	45366001
Subset member	450828004~ACCEPTABILITYID~900000000000549004 450828004~ACCEPTABILITYID~900000000000548007
tui	T047
Type ID	900000000000003001 900000000000013009
subClassOf	http://purl.bioontology.org/ontology/SCTSPA/111589005 http://purl.bioontology.org/ontology/SCTSPA/31925001

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MEDDRA/10051123	MEDDRA	CUI
http://purl.bioontology.org/ontology/OMIM/616004	OMIM	CUI
http://purl.bioontology.org/ontology/ICD10CM/D68.2	ICD10CM	CUI
http://purl.bioontology.org/ontology/SNMI/DC-64010	SNMI	CUI
http://purl.bioontology.org/ontology/MDRGER/10051123	MDRGER	CUI
http://purl.bioontology.org/ontology/MDRFRE/10054362	MDRFRE	CUI
http://purl.bioontology.org/ontology/MDRFRE/10051123	MDRFRE	CUI
http://purl.bioontology.org/ontology/MDRGER/10054362	MDRGER	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/45366001	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/MEDDRA/10054362	MEDDRA	CUI
http://purl.bioontology.org/ontology/MESH/C562727	MESH	CUI