OMOP Concept 4259712
Heterozygous protein S deficiency
StandardConditionSNOMED440988005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2009
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Heterozygous protein S deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 156610 | Heterozygous protein S deficiency | Non-standard |
Synonyms
Alternative names recorded for Heterozygous protein S deficiency across source vocabularies.
- deficiencia heterocigota de proteína S
- deficiencia heterocigota de proteína S (trastorno)
- Heterozygous protein S 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 S deficiency
- 2Hereditary thrombophilia
- 2Protein S 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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