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loading...| Preferred Name |
Factor V Deficiency [Disease/Finding] |
|
| Synonyms |
Labile Factor Deficiency |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001199 |
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| altLabel |
Labile Factor Deficiency Factor V Deficiency Owren's Disease Owren Parahemophilia Owren Disease Deficiency, Factor V Parahemophilia |
|
| cui |
C0015499 |
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| 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) |
|
| MESH DUI |
D005166 |
|
| MeSH name |
Factor V Deficiency |
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| MESH UI |
M0008143 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000001199 |
|
| NUI |
N0000001199 |
|
| prefLabel |
Factor V Deficiency [Disease/Finding] |
|
| SNOMED CID |
88776002 4320005 365157004 366160003 |
|
| tui |
T047 |
|
| subClassOf |
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