1254946006: Hypopigmentation-immunodeficiency disease type 1 (disorder)

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

Status: current, Primitive. Date: 31-Oct 2022. Module: SNOMED CT core

Descriptions:

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

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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