National Cancer Institute Thesaurus

Last uploaded: February 21, 2019

Preferred Name	Factor I Deficiency
ID	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26692
code	C26692
DEFINITION	A usually inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding.
FULL_SYN	Fibrinogen Deficiency
label	Factor I Deficiency
Legacy_Concept_Name	Factor_I_Deficiency
NCI_META_CUI	CL480897
Preferred_Name	Factor I Deficiency
prefixIRI	C26692
prefLabel	Factor I Deficiency
Semantic_Type	Disease or Syndrome
subClassOf	http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C27215

Delete	Subject	Author	Type	Created
No notes to display

Delete	Mapping To	Ontology	Source
	There are currently no mappings for this class.