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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Preferred Name | Factor V Deficiency [Disease/Finding] | |
| Synonyms |
Labile Factor Deficiency Factor V Deficiency Owren's Disease Owren Parahemophilia Owren Disease Deficiency, Factor V Parahemophilia |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001199 |
|
| altLabel |
Labile Factor Deficiency Factor V Deficiency Owren's Disease Owren Parahemophilia Owren Disease Deficiency, Factor V Parahemophilia
|
|
| cui |
C0015499
|
|
| MESH DEFINITION |
A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia. It varies greatly in severity. Factor V deficiency is an autosomal recessive trait. (Dorland, 27th ed)
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|
| MESH DUI |
D005166
|
|
| MeSH name |
Factor V Deficiency
|
|
| MESH UI |
M0008143
|
|
| NDFRT kind |
DISEASE_KIND
|
|
| notation |
N0000001199
|
|
| NUI |
N0000001199
|
|
| prefLabel |
Factor V Deficiency [Disease/Finding]
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|
| SNOMED CID |
88776002 4320005 365157004 366160003
|
|
| tui |
T047
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|
| subClassOf |
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