OMOP Concept 37397560
Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
StandardConditionSNOMED718230004Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535530 | Interferon gamma, receptor 1, deficiency | Non-standard |
Synonyms
Alternative names recorded for Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency across source vocabularies.
- Mendelian susceptibility to mycobacterial disease due to complete IFNgammaR1 deficiency
- Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency (disorder)
- susceptibilidad mendeliana a enfermedad por micobacterias debida a deficiencia completa de receptor 1 de interferón gamma
- susceptibilidad mendeliana a enfermedad por micobacterias debida a deficiencia completa de receptor 1 de interferón gamma (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
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