234639001: Triple X syndrome, epilepsy, and hypogammaglobulinemia (disorder)

• SNOMED CT Concept\constatation clinique\Disease\...
• \trouble de la fonction immunitaire\troubles d'immunodéficience\Primary immune deficiency disorder (disorder)\Immunodeficiency associated with chromosomal abnormality\Triple X syndrome, epilepsy, and hypogammaglobulinemia
• \affection d'un système corporel\Disorder of immune structure (disorder)\Triple X syndrome, epilepsy, and hypogammaglobulinemia

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
351581014	Triple X syndrome, epilepsy, and hypogammaglobulinemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
351582019	Triple X syndrome, epilepsy, and hypogammaglobulinaemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
622986015	Triple X syndrome, epilepsy, and hypogammaglobulinemia (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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