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.

VocabularyCodeNameType
MeSHC535530Interferon gamma, receptor 1, deficiencyNon-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.

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