loading...| Preferred Name |
Thrombophilia due to Activated Protein C Resistance |
|
| Synonyms |
Thrombophilia due to Deficiency of Activated Protein C Cofactor |
|
| ID |
http://purl.bioontology.org/ontology/MESH/C566056 |
|
| altLabel |
Thrombophilia due to Deficiency of Activated Protein C Cofactor Factor V Leiden Thrombophilia Thrombophilia due to Factor V Leiden Protein C Cofactor Deficiency Hereditary Resistance To Activated Protein C Apc Resistance, Leiden Type Thrombophilia V |
|
| cui |
C1861171 |
|
| HM |
D020016 |
|
| Inverse of RB |
0 |
|
| Mapped to | ||
| MDA |
20121105 |
|
| MeSH Frequency |
63 |
|
| MMR |
20150818 |
|
| notation |
C566056 |
|
| prefLabel |
Thrombophilia due to Activated Protein C Resistance |
|
| SC |
3 |
|
| Scope Statement |
A hereditary autosomal dominant susceptibility for THROMBOSIS that is caused by mutations in the F5 gene, resulting in factor V resistant to cleavage and inactivation by activated PROTEIN C. OMIM: 188055 |
|
| TERMUI |
T807843 T841360 T826397 T826392 T841359 T826391 T841358 T826390 |
|
| TH |
OMIM (2013) GHR (2014) |
|
| tui |
T047 |