OMOP Concept 4209490
Heterozygous protein C deficiency
StandardConditionSNOMED441101007Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2009
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Heterozygous protein C deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 156609 | Heterozygous protein C deficiency | Non-standard |
| Nebraska Lexicon | 441101007 | Heterozygous protein C deficiency | Non-standard |
Synonyms
Alternative names recorded for Heterozygous protein C deficiency across source vocabularies.
- deficiencia heterocigota de proteína C
- deficiencia heterocigota de proteína C (trastorno)
- Heterozygous protein C deficiency (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Hereditary protein C deficiency
- 2Hereditary thrombophilia
- 2Protein C deficiency disease
- 3Deficiency of naturally occurring coagulation factor inhibitor
- 3Hereditary disease
- 3Thrombophilia
- 4Blood coagulation disorder
- 4Disorder of hemostatic system
- 4Genetic disease
- 5Disease
- 5Functional finding
- 5OMOP Bleeding 1
- 5OMOP Bleeding 2
- 6Clinical finding
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