22406001: Severe combined immunodeficiency due to absent lymphoid stem cells (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 lymphoid stem cells (disorder)

\Disorder of immune function (disorder)\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent lymphoid stem cells (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 lymphoid stem cells (disorder)
\Disorder of immune function (disorder)\Immunodeficiency disorder\Congenital immunodeficiency disease\Congenital agammaglobulinemia\Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)
\Disorder of immune function (disorder)\Immunodeficiency disorder\Congenital immunodeficiency disease\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)

\Disorder of body system\Hereditary disorder by system\Hereditary disorder of immune system\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)

\Congenital disease (disorder)\Congenital immunodeficiency disease\...

\Congenital agammaglobulinemia\Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)

\Severe combined immunodeficiency disease\Severe combined immunodeficiency due to absent lymphoid stem cells (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 lymphoid stem cells (disorder)	Is a	Congenital agammaglobulinemia	true	Inferred relationship	Some
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	Is a	Congenital anomaly of the hematopoietic system	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	Is a	Severe combined immunodeficiency disease	true	Inferred relationship	Some
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	Is a	Bone marrow disorder	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	Finding site	Structure of immune system (body structure)	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	Severity	Severe (severity modifier) (qualifier value)	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	Finding site	Stem cell	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	Is a	Hereditary disorder of hematologic system	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	Has definitional manifestation	Immune system finding	false	Inferred relationship	Some
Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	Finding site	Body system structure	true	Inferred relationship	Some	1
Severe combined immunodeficiency due to absent lymphoid stem cells (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

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Id	Description	Lang	Type	Status	Case?	Module
37615016	Swiss type agammaglobulinemia	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
481336016	Agammaglobulinaemia - Swiss type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2914257016	Severe combined immunodeficiency due to absent lymphoid stem cells	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2914977019	Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5247167011	SCID (severe combined immunodeficiency) due to absent lymphoid stem cells	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4663431000172119	'severe combined immunodeficiency' door afwezigheid van lymfoïde stamcellen	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4663441000172114	SCID door afwezigheid van lymfoïde stamcellen	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
4663451000172111	ernstige gecombineerde immuundeficiëntie door afwezigheid van lymfoïde stamcellen	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4663461000172113	ernstige gecombineerde immunodeficiëntie door afwezigheid van lymfoïde stamcellen	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)