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loading...| Preferred Name |
Protein C Deficiency [Disease/Finding] |
|
| Synonyms |
Hereditary Thrombophilia Due To Protein C Deficiency |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000004007 |
|
| altLabel |
Hereditary Thrombophilia Due To Protein C Deficiency Deficiency, Protein C Protein C Deficiency |
|
| cui |
C0398625 |
|
| May be treated by |
http://purl.bioontology.org/ontology/NDFRT/N0000191329 |
|
| MESH DEFINITION |
An absence or deficiency in PROTEIN C which leads to impaired regulation of blood coagulation. It is associated with an increased risk of severe or premature thrombosis. (Stedman's Med. Dict., 26th ed.) |
|
| MESH DUI |
D020151 |
|
| MeSH name |
Protein C Deficiency |
|
| MESH UI |
M0029882 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000004007 |
|
| NUI |
N0000004007 |
|
| prefLabel |
Protein C Deficiency [Disease/Finding] |
|
| SNOMED CID |
76407009 |
|
| tui |
T047 |
|
| subClassOf |
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