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Biological and Environmental Research Ontology
Last uploaded:
December 23, 2022
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| Preferred Name | Hereditary Factor XI Deficiency | |
| Synonyms |
|
|
| Definitions |
A rare inherited bleeding disorder caused by deficiency of coagulation factor XI. It may be asymptomatic or manifest with bleeding. |
|
| ID |
http://purl.obolibrary.org/obo/NCIT_C84705 |
|
| ALT_DEFINITION |
An autosomal recessive, inherited coagulation disorder characterized by the partial or complete absence of factor XI activity in the blood.
|
|
| code |
C84705
|
|
| Contributing_Source |
NICHD
|
|
| definition |
A rare inherited bleeding disorder caused by deficiency of coagulation factor XI. It may be asymptomatic or manifest with bleeding.
|
|
| in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 |
|
| label |
Hereditary Factor XI Deficiency
|
|
| Preferred_Name |
Hereditary Factor XI Deficiency
|
|
| prefixIRI |
NCIT:C84705
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|
| prefLabel |
Hereditary Factor XI Deficiency
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|
| Semantic_Type |
Disease or Syndrome
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|
| UMLS_CUI |
C0015523
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|
| subClassOf |
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