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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Preferred Name | Factor XI Deficiency [Disease/Finding] | |
| Synonyms |
Rosenthal Syndrome Hemophilia C Plasma Thromboplastin Antecedent Deficiency Deficiency, Factor XI Rosenthal's Syndrome Factor XI Deficiency |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001202 |
|
| altLabel |
Rosenthal Syndrome Hemophilia C Plasma Thromboplastin Antecedent Deficiency Deficiency, Factor XI Rosenthal's Syndrome Factor XI Deficiency
|
|
| cui |
C0015523
|
|
| MESH DEFINITION |
A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia.
|
|
| MESH DUI |
D005173
|
|
| MeSH name |
Factor XI Deficiency
|
|
| MESH UI |
M0008157
|
|
| NDFRT kind |
DISEASE_KIND
|
|
| notation |
N0000001202
|
|
| NUI |
N0000001202
|
|
| prefLabel |
Factor XI Deficiency [Disease/Finding]
|
|
| SNOMED CID |
49762007
|
|
| tui |
T047
|
|
| subClassOf |
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