234638009: Microcephaly, normal intelligence and immunodeficiency (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Genetic disease\Hereditary disease\...
• \Hereditary neoplastic syndrome\Microcephaly, normal intelligence and immunodeficiency
• \Hereditary disorder by system\Hereditary disorder of immune system\Microcephaly, normal intelligence and immunodeficiency
• \Disorder of immune function\Hereditary disorder of immune system\Microcephaly, normal intelligence and immunodeficiency
• \Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Immunodeficiency associated with chromosomal abnormality\Microcephaly, normal intelligence and immunodeficiency
• \Disorder of body system\Disorder of immune structure\Microcephaly, normal intelligence and immunodeficiency
• \Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Microcephaly, normal intelligence and immunodeficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
351577014	Microcephaly, normal intelligence and immunodeficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
351578016	Nijmegen breakage syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
351579012	NBS - Nijmegen breakage syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
351580010	Seemanova syndrome II	en	Synonym	Active	Case sensitive	SNOMED CT core
622985016	Microcephaly, normal intelligence and immunodeficiency (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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