Pediatric Terminology

Last uploaded: January 25, 2013

Preferred Name	Hereditary_Factor_II_Deficiency_Disease
Synonyms
ID	http://www.owl-ontologies.com/Ontology1358660052.owl#Hereditary_Factor_II_Deficiency_Disease
ID	C26799
NCI_Definition	A very rare autosomal recessive inherited blood coagulation disorder characterized by deficiency of prothrombin, resulting in bleeding.
NCI_PT	Hereditary Factor II Deficiency
NICHD_Definition	_
prefixIRI	Hereditary_Factor_II_Deficiency_Disease
prefLabel	Hereditary_Factor_II_Deficiency_Disease
Subset_Association1	NICHD Pediatric Terminology
Subset_Association2	Neonatal Research Network Terminology
SYN
subClassOf	http://www.owl-ontologies.com/Ontology1358660052.owl#Hereditary_Coagulation_Factor_Deficiency

Delete	Subject	Author	Type	Created
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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/SNOMEDCT/33297000	SNOMEDCT	LOOM
	http://purl.bioontology.org/ontology/SNMI/DC-63030	SNMI	LOOM