OMOP Concept 4289831
SCID (severe combined immunodeficiency) due to absent adenosine deaminase
StandardConditionSNOMED36980009Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to SCID (severe combined immunodeficiency) due to absent adenosine deaminase via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 127111 | SCID due to Absent Adenosine Deaminase | Non-standard |
Synonyms
Alternative names recorded for SCID (severe combined immunodeficiency) due to absent adenosine deaminase across source vocabularies.
- inmunodeficiencia combinada severa por ausencia de adenosina deaminasa
- inmunodeficiencia combinada severa por ausencia de adenosina desaminasa
- inmunodeficiencia combinada severa por ausencia de adenosina desaminasa (trastorno)
- SCID (inmunodeficiencia combinada severa) por ausencia de ADA (adenosina desaminasa)
- SCID (severe combined immunodeficiency) due to absent ADA (adenosine deaminase)
- Severe combined immunodeficiency due to absent adenosine deaminase
- Severe combined immunodeficiency due to absent adenosine deaminase (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Severe combined immunodeficiency disease
- 2Combined immunodeficiency disease
- 2Congenital immunodeficiency disease
- 2Hereditary disorder of immune system
- 3Congenital disease
- 3Disorder of immune function
- 3Hereditary disorder by system
- 3Immunodeficiency disorder
- 3Primary immune deficiency disorder
- 4Disease
- 4Disorder of body system
- 4Fetal and/or neonatal disorder
- 4Hereditary disease
- 5Clinical finding
- 5Genetic disease
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