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

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

Descriptions:

Id Description Lang Type Status Case? Module
351581014 Triple X syndrome, epilepsy, and hypogammaglobulinemia en Synonym Active Entire term case sensitive SNOMED CT core module
351582019 Triple X syndrome, epilepsy, and hypogammaglobulinaemia en Synonym Active Entire term case sensitive SNOMED CT core module
622986015 Triple X syndrome, epilepsy, and hypogammaglobulinemia (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core 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
Triple X syndrome, epilepsy, and hypogammaglobulinemia Finding site Structure of immune system true Inferred relationship Existential restriction modifier 1
Triple X syndrome, epilepsy, and hypogammaglobulinemia Is a Disorder of immune structure true Inferred relationship Existential restriction modifier
Triple X syndrome, epilepsy, and hypogammaglobulinemia Associated with Chromosomal disorder true Inferred relationship Existential restriction modifier 2
Triple X syndrome, epilepsy, and hypogammaglobulinemia Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier
Triple X syndrome, epilepsy, and hypogammaglobulinemia Pathological process Abnormal immune process true Inferred relationship Existential restriction modifier 3
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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