71904008: Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)

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

\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)

\Disorder of immune function (disorder)\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)
\Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)
\Disorder of immune function (disorder)\Immunodeficiency disorder\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)

\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)

\Congenital disease (disorder)\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)	Is a	Severe combined immunodeficiency disease	true	Inferred relationship	Some
Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)	Severity	Severe (severity modifier) (qualifier value)	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)	Finding site	Lymphocyte	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)	Finding site	Structure of immune system (body structure)	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)	Is a	Disorder of immune structure (disorder)	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)	Has definitional manifestation	Immune system finding	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)	Finding site	Body system structure	true	Inferred relationship	Some	1
Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)	Pathological process (attribute)	Abnormal immune process (qualifier value)	true	Inferred relationship	Some	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
119476015	Bare lymphocyte syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2914021019	Severe combined immunodeficiency due to absent class II human leukocyte antigens (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2914447015	Severe combined immunodeficiency due to absent class II human leukocyte antigens	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5247168018	SCID (severe combined immunodeficiency) due to absent class II HLA (human leukocyte antigens)	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5247169014	BLS - bare lymphocyte syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4136791000172114	SCID door afwezigheid van HLA klasse II	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
4136801000172110	'severe combined immunodeficiency' door afwezigheid van humane leukocytenantigenen klasse II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
4136811000172113	'bare lymphocyte'-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4136821000172115	ernstige gecombineerde immuundeficiëntie door afwezigheid van humane leukocytenantigenen klasse II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
4136831000172117	ernstige gecombineerde immunodeficiëntie door afwezigheid van humane leukocytenantigenen klasse II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)