Systematized Nomenclature of Medicine, International Version

Last uploaded: January 31, 2024

Preferred Name	Hereditary factor V deficiency disease
Synonyms	Hereditary hypoproaccelerinemia
ID	http://purl.bioontology.org/ontology/SNMI/DC-63060
altLabel	Hereditary hypoproaccelerinemia Owren's disease AC globulin deficiency Labile factor deficiency Parahemophilia
cui	C0015499
notation	DC-63060
prefLabel	Hereditary factor V deficiency disease
SIC	286.3
tui	T047
subClassOf	http://purl.bioontology.org/ontology/SNMI/DC-63000

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/ICD10CM/D68.2	ICD10CM	CUI
http://purl.bioontology.org/ontology/RCD/D3032	RCD	CUI
http://purl.bioontology.org/ontology/NDFRT/N0000001199	NDFRT	CUI
http://purl.bioontology.org/ontology/MESH/D005166	MESH	CUI
http://purl.bioontology.org/ontology/OMIM/227400	OMIM	CUI
http://purl.bioontology.org/ontology/SCTSPA/88776002	SCTSPA	CUI
http://purl.bioontology.org/ontology/MSHFRE/D005166	MSHFRE	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/88776002	SNOMEDCT	CUI
http://www.owl-ontologies.com/Ontology1358660052.owl#Hereditary_Factor_V_Deficiency_Disease	PEDTERM	LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/88776002	SNOMEDCT	LOOM