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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Preferred Name | Factor X Deficiency [Disease/Finding] | |
| Synonyms |
Stuart-Prower Deficiency Stuart-Prower Factor Deficiency Deficiency, Factor X Deficiency, Stuart-Prower Deficiency, Stuart-Prower Factor Factor X Deficiency |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001201 |
|
| altLabel |
Stuart-Prower Deficiency Stuart-Prower Factor Deficiency Deficiency, Factor X Deficiency, Stuart-Prower Deficiency, Stuart-Prower Factor Factor X Deficiency
|
|
| cui |
C0015519
|
|
| MESH DEFINITION |
Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
|
|
| MESH DUI |
D005171
|
|
| MeSH name |
Factor X Deficiency
|
|
| MESH UI |
M0008155
|
|
| NDFRT kind |
DISEASE_KIND
|
|
| notation |
N0000001201
|
|
| NUI |
N0000001201
|
|
| prefLabel |
Factor X Deficiency [Disease/Finding]
|
|
| SNOMED CID |
76642003
|
|
| tui |
T047
|
|
| subClassOf |
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