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Pediatric Terminology
Last uploaded:
January 25, 2013
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| Preferred Name | Hereditary_Factor_XI_Deficiency_Disease | |
| Synonyms |
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| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Hereditary_Factor_XI_Deficiency_Disease |
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| ID |
C84705
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| NCI_Definition |
A rare inherited bleeding disorder caused by deficiency of coagulation factor XI. It may be asymptomatic or manifest with bleeding.
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| NCI_PT |
Hereditary Factor XI Deficiency
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| NICHD_Definition |
_
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| prefixIRI |
Hereditary_Factor_XI_Deficiency_Disease
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| prefLabel |
Hereditary_Factor_XI_Deficiency_Disease
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| Subset_Association1 |
NICHD Pediatric Terminology
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| Subset_Association2 |
Neonatal Research Network Terminology
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| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Autosomal_Recessive_Hereditary_Disorder |
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| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
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| Mapping To | Ontology | Source |
|---|---|---|
| http://purl.bioontology.org/ontology/SNOMEDCT/49762007 | SNOMEDCT | LOOM |
| http://purl.bioontology.org/ontology/SNMI/DC-63240 | SNMI | LOOM |