1179288008: Combined immunodeficiency due to transferrin receptor deficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Combined immunodeficiency due to transferrin receptor deficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Combined immunodeficiency due to transferrin receptor 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
4650559015	Combined immunodeficiency due to transferrin receptor deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
4650560013	Combined immunodeficiency due to transferrin receptor deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4650567011	TFRC (transferrin receptor) related combined immunodeficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
4650568018	Combined immunodeficiency due to TFRC deficiency	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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