55602000: Nezelof's syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Nezelof's syndrome
• \Disorder of immune function\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Nezelof's syndrome
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Severe combined immunodeficiency disease\Nezelof's syndrome
• \Disorder of immune function\Immunodeficiency disorder\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Nezelof's syndrome
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Nezelof's syndrome
• \Congenital disease\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Nezelof's syndrome

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2840435013	Nezelof syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
793991019	Nezelof's syndrome (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
92425010	Nezelof's syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
92426011	Congenital thymic dysplasia syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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