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723384004: Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3424323018 Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3424324012 Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3424325013 Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3424326014 Mendelian susceptibility to mycobacterial disease due to complete ISG15 (interferon stimulated gene 15) deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency Due to Chromosomal disorder false Inferred relationship Existential restriction modifier 1
Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency Is a Immunodeficiency associated with chromosomal abnormality false Inferred relationship Existential restriction modifier
Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 2
Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency Is a Mendelian susceptibility to mycobacterial disease true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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