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765188009: Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3657381018 Severe combined immunodeficiency due to complete RAG1 (recombination activating gene 1) and/or RAG2 (recombination activating gene 2) deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3657382013 SCID (severe combined immunodeficiency) due to complete RAG1/2 deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
3657384014 Severe combined immunodeficiency due to complete RAG1 and/or RAG2 deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
3657386011 Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency en Synonym Active Entire term case insensitive SNOMED CT core module
3657387019 Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency Finding site Structure of immune system true Inferred relationship Existential restriction modifier 1
Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency Is a Severe combined immunodeficiency with low T- and B-cell numbers true Inferred relationship Existential restriction modifier
Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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