1179286007: Combined immunodeficiency due to GINS complex subunit 1 deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined immunodeficiency due to GINS complex subunit 1 deficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Combined immunodeficiency due to GINS complex subunit 1 deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Oct 2021. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4650548012	Combined immunodeficiency due to GINS1 (GINS complex subunit 1) deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4650550016	Combined immunodeficiency due to GINS complex subunit 1 deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4650551017	Combined immunodeficiency due to GINS complex subunit 1 deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
4650552012	Combined immunodeficiency due to GINS1 deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
4650553019	Combined immunodeficiency with intrauterine growth retardation, NK (natural killer) cell deficiency, neutropenia	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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