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

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
351581014 Triple X syndrome, epilepsy, and hypogammaglobulinemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character case insensitive (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
4997581000241115 syndrome du triple X, épilepsie et hypogammaglobulinémie fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4997581000241115 syndrome du triple X, épilepsie et hypogammaglobulinémie fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Triple X syndrome, epilepsy, and hypogammaglobulinemia Is a Immunodeficiency associated with chromosomal abnormality true Inferred relationship Existential restriction modifier (core metadata concept)
Triple X syndrome, epilepsy, and hypogammaglobulinemia Finding site Structure of immune system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Triple X syndrome, epilepsy, and hypogammaglobulinemia Is a Disorder of immune structure true Inferred relationship Existential restriction modifier (core metadata concept)
Triple X syndrome, epilepsy, and hypogammaglobulinemia Associated with Chromosomal disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Triple X syndrome, epilepsy, and hypogammaglobulinemia Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
Triple X syndrome, epilepsy, and hypogammaglobulinemia Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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