OMOP Concept 4125650
Thrombophilia
StandardConditionSNOMED234467004Disorder
Maps from
14
Descendants
55
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
14 source codes normalize to Thrombophilia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 153674 | Thrombophilia | Non-standard |
| CIM10 | D68.6 | Other thrombophilia | Non-standard |
| ICD10 | D68.6 | Other thrombophilia | Non-standard |
| ICD10CM | D68.6 | Other thrombophilia | Non-standard |
| ICD10CM | D68.69 | Other thrombophilia | Non-standard |
| ICD10CN | D68.6 | Other thrombophilia | Non-standard |
| ICD10CN | D68.600 | Other thrombophilia | Non-standard |
| ICD10CN | D68.601 | Anticardiolipin antibody syndrome (machine translation) | Non-standard |
| ICD10CN | D68.602 | Ekisensho (machine translation) | Non-standard |
| ICD10GM | D68.6 | Other thrombophilia | Non-standard |
| KCD7 | D68.6 | Other thrombophilia | Non-standard |
| MeSH | D019851 | Thrombophilia | Non-standard |
| Nebraska Lexicon | 234467004 | Thrombophilia | Non-standard |
| Read | D30A.00 | Thrombophilia | Non-standard |
Synonyms
Alternative names recorded for Thrombophilia across source vocabularies.
- Thrombophilia (disorder)
- trombofilia
- trombofilia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(55)Included automatically when you query with descendants.
- 1Acquired thrombophilia
- 1Antithrombin III deficiency
- 1Heparin cofactor II deficiency
- 1Hereditary thrombophilia
- 1Protein C deficiency disease
- 1Protein S deficiency disease
- 1Thrombophilia associated with pregnancy
- 1Thrombophilia due to vascular anomaly
- 2Acquired antithrombin III deficiency
- 2Acquired heparin cofactor II deficiency
- 2Acquired protein C deficiency
- 2Acquired protein S deficiency
- 2Antiphospholipid syndrome
- 2Antiphospholipid syndrome in pregnancy
- 2Antithrombin III deficiency type I
- 2Antithrombin III deficiency type II
- 2Factor V Leiden mutation
- 2Hereditary antithrombin III deficiency
- 2Hereditary elevated factor VIII
- 2Hereditary elevated factor XI
- 2Hereditary heparin cofactor II deficiency
- 2Hereditary hyperfibrinogenemia
- 2Hereditary hyperhomocysteinemia
- 2Hereditary protein C deficiency
- 2Hereditary protein S deficiency
- 2Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
- 2Hereditary thrombophilic dysfibrinogenemia
- 2Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
- 2Prothrombin G20210A mutation
- 2Resistance to activated protein C due to factor V Leiden mutation
- 2Thrombophilia caused by vascular device
- 2Thrombophilia due to antineoplastic agent therapy
- 2Thrombophilia due to hormone therapy
- 2Thrombophilia due to immobilization
- 2Thrombophilia due to malignant neoplasm
- 2Thrombophilia due to myeloproliferative disorder
- 2Thrombophilia due to paroxysmal nocturnal hemoglobinuria
- 2Thrombophilia due to trauma
- 3Catastrophic antiphospholipid syndrome
- 3Heterozygous Factor V Leiden mutation
- 3Heterozygous protein C deficiency
- 3Heterozygous protein S deficiency
- 3Heterozygous prothrombin G20210A mutation
- 3Homozygous Factor V Leiden mutation
- 3Homozygous protein C deficiency
- 3Homozygous protein S deficiency
- 3Homozygous prothrombin G20210A mutation
- 3Lupus anticoagulant disorder
- 3Neonatal antiphospholipid syndrome
- 3Primary antiphospholipid syndrome
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