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191012007: Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (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
293721011 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
574662018 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
293721011 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
574662018 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4848121000241112 déficit immunitaire commun variable avec anomalie prédominante en lymphocytes T immunorégulateurs fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4848121000241112 déficit immunitaire commun variable avec anomalie prédominante en lymphocytes T immunorégulateurs 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
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Is a Common variable agammaglobulinaemia false Inferred relationship Existential restriction modifier (core metadata concept)
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Finding site Structure of immune system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Is a Disorder of immune structure false Inferred relationship Existential restriction modifier (core metadata concept)
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Is a Hereditary disorder of immune system false Inferred relationship Existential restriction modifier (core metadata concept)
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder) Is a Common variable immunodeficiency true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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