234635007: Chromosome 22 abnormalities with hypogammaglobulinemia (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\Immunodeficiency associated with chromosomal abnormality\Chromosome 22 abnormalities with hypogammaglobulinaemia

\Disorder of body system\Disorder of immune structure\Chromosome 22 abnormalities with hypogammaglobulinaemia

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

351572015 Chromosome 22 abnormalities with hypogammaglobulinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

351573013 Chromosome 22 abnormalities with hypogammaglobulinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

622981013 Chromosome 22 abnormalities with hypogammaglobulinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

351572015 Chromosome 22 abnormalities with hypogammaglobulinaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

351572015 Chromosome 22 abnormalities with hypogammaglobulinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

351573013 Chromosome 22 abnormalities with hypogammaglobulinemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

351573013 Chromosome 22 abnormalities with hypogammaglobulinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

622981013 Chromosome 22 abnormalities with hypogammaglobulinemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

622981013 Chromosome 22 abnormalities with hypogammaglobulinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4997541000241112 anomalie du chromosome 22 associé à une hypogammaglobulinémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

4997541000241112 anomalie du chromosome 22 associé à une hypogammaglobulinémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Chromosome 22 abnormalities with hypogammaglobulinaemia	Is a	Immunodeficiency associated with chromosomal abnormality	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Chromosome 22 abnormalities with hypogammaglobulinaemia	Finding site	Structure of immune system (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Chromosome 22 abnormalities with hypogammaglobulinaemia	Is a	Disorder of immune structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Chromosome 22 abnormalities with hypogammaglobulinaemia	Associated with	Chromosomal disorder (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Chromosome 22 abnormalities with hypogammaglobulinaemia	Has definitional manifestation	Immune system finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Chromosome 22 abnormalities with hypogammaglobulinaemia	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
Monosomy 22 and absence of immunoglobulin A	Is a	True	Chromosome 22 abnormalities with hypogammaglobulinaemia	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets