OMOP Concept 37397461
T-cell negative B-cell positive severe combined immunodeficiency due to JAK3 deficiency
StandardConditionSNOMED718107000Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to T-cell negative B-cell positive severe combined immunodeficiency due to JAK3 deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563440 | Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative | Non-standard |
| Nebraska Lexicon | 718107000 | Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency | Non-standard |
Synonyms
Alternative names recorded for T-cell negative B-cell positive severe combined immunodeficiency due to JAK3 deficiency across source vocabularies.
- inmunodeficiencia combinada severa negativa para linfocitos T, positiva para linfocitos B debida a deficiencia de cinasa jano-3
- inmunodeficiencia combinada severa negativa para linfocitos T, positiva para linfocitos B debida a deficiencia de cinasa jano-3 (trastorno)
- inmunodeficiencia combinada severa negativa para linfocitos T, positiva para linfocitos B debida a deficiencia de JAK3
- Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency
- Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(19)Roll up to these when you need a wider cohort.
- 1Autosomal recessive SCID (severe combined immunodeficiency disease)
- 1T-cell negative B-cell positive severe combined immunodeficiency
- 2Autosomal recessive hereditary disorder
- 2Severe combined immunodeficiency disease
- 3Autosomal hereditary disorder
- 3Combined immunodeficiency disease
- 3Congenital immunodeficiency disease
- 3Hereditary disorder of immune system
- 4Congenital disease
- 4Disorder of immune function
- 4Hereditary disease
- 4Hereditary disorder by system
- 4Immunodeficiency disorder
- 4Primary immune deficiency disorder
- 5Disease
- 5Disorder of body system
- 5Disorder of fetus and/or newborn
- 5Genetic disease
- 6Clinical finding
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