723385003: Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Mendelian susceptibility to mycobacterial disease\Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency
• \Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Mendelian susceptibility to mycobacterial disease\Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency

Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3424331011	Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3424332016	Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
3424333014	Mendelian susceptibility to mycobacterial disease due to partial IRF8 (interferon regulatory factor 8) deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3424334015	Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3424335019	A rare genetic variant of mendelian susceptibility to mycobacterial disease with characteristics of selective susceptibility to relatively mild infections with bacillus Calmette-Guerin (BCG). The prevalence is unknown. The first infections occur after vaccination with BCG and before the age of 2. No other infectious diseases have been reported. Caused by heterozygous mutations in the IRF8 gene on chromosome 16q24.1 which encodes IRF8, a protein essential for the development of dendritic cells and the differentiation of macrophages and granulocytes. Mutations in the IRF8 gene impair IL-12 secretion by monocytes and dendritic cells. Inherited in an autosomal dominant manner.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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