Hereditary thrombophilia (Q39591): Difference between revisions
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Revision as of 05:04, 13 August 2026
A disease caused by hereditary factors leading to abnormalities in blood. This disease is characterised by abnormality of blood coagulation that increases the risk of thrombosis, clots in blood vessels. This disease may present with deep vein thrombosis or pulmonary embolism. Confirmation is identification of abnormal blood coagulation in a blood sample.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B61.0 |
||
| English | Hereditary thrombophilia |
A disease caused by hereditary factors leading to abnormalities in blood. This disease is characterised by abnormality of blood coagulation that increases the risk of thrombosis, clots in blood vessels. This disease may present with deep vein thrombosis or pulmonary embolism. Confirmation is identification of abnormal blood coagulation in a blood sample. |
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CID11:3B61.0
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dki-india-3B61.0
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