1254946006: Hypopigmentation-immunodeficiency disease type 1 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Disorder of pigmentation\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 1
• \Disorder of immune function\Immunodeficiency disorder\...
• \Primary immune deficiency disorder\Immunodeficiency with major anomalies\Immunodeficiency associated with multiple organ system abnormalities\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 1
• \Congenital immunodeficiency disease\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 1
• \Disorder of body system\Disorder of immune structure\Immunodeficiency with major anomalies\Immunodeficiency associated with multiple organ system abnormalities\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 1
• \Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of tyrosine metabolism\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 1
• \Congenital disease\Congenital malformation\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 1
• \Congenital disease\Congenital immunodeficiency disease\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 1
• \Developmental disorder\Congenital malformation\Hypopigmentation-immunodeficiency disease\Hypopigmentation-immunodeficiency disease type 1

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Oct 2022. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5143922017	Hypopigmentation-immunodeficiency disease type 1 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
5143923010	Griscelli syndrome type 1	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
5146507013	Hypopigmentation-immunodeficiency disease type 1	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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