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Terminology chevron_right Concepts chevron_right 3439009

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Component

3439009

The component that hold information about this concept.

Fully Specified Name (FSN)

Severe combined immunodeficiency due to absent peripheral t cell maturation (disorder)

Shortest Term

Scid due to absent peripheral t cell maturation

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Severe combined immunodeficiency due to absent peripheral t cell maturation (disorder)

SCTID: 3439009, Primitive, Active

3439009|Severe combined immunodeficiency due to absent peripheral t cell maturation (disorder)|

en Scid (severe combined immunodeficiency) due to absent peripheral t cell maturation
en Combined immunodeficiency associated with maturation pathway defect
en Severe combined immunodeficiency due to absent peripheral t cell maturation
en Severe combined immunodeficiency due to absent peripheral t cell maturation (disorder)

Expression

3439009 |Severe combined immunodeficiency due to absent peripheral t cell maturation (disorder)|
 <<< 31323000 |Severe combined immunodeficiency disease (disorder)| : 
        { 363698007 |Finding site (attribute)| = 91689009 |Body system structure (body structure)| }
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
6812016 - SCID due to absent peripheral T cell maturation (en) View
6812016	en	Synonym (core metadata concept)	SCID due to absent peripheral T cell maturation	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False
5247170010 - SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation (en) View
5247170010	en	Synonym (core metadata concept)	SCID (severe combined immunodeficiency) due to absent peripheral T cell maturation	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
2620625016 - Severe combined immunodeficiency (SCID) due to absent peripheral T cell maturation (en) View
2620625016	en	Synonym (core metadata concept)	Severe combined immunodeficiency (SCID) due to absent peripheral T cell maturation	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
485833013 - Combined immunodeficiency associated with maturation pathway defect (en) View
485833013	en	Synonym (core metadata concept)	Combined immunodeficiency associated with maturation pathway defect	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2913244019 - Severe combined immunodeficiency due to absent peripheral T cell maturation (en) View
2913244019	en	Synonym (core metadata concept)	Severe combined immunodeficiency due to absent peripheral T cell maturation	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
2914606012 - Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder) (en) View
2914606012	en	Fully specified name (core metadata concept)	Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2612232013 - Severe combined immunodeficiency (SCID) due to absent peripheral T cell maturation (disorder) (en) View
2612232013	en	Fully specified name (core metadata concept)	Severe combined immunodeficiency (SCID) due to absent peripheral T cell maturation (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
765908010 - SCID due to absent peripheral T cell maturation (disorder) (en) View
765908010	en	Fully specified name (core metadata concept)	SCID due to absent peripheral T cell maturation (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (757837023) - 3439009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2731539020) - 3439009 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11171153023) - 3439009 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2731540022) - 3439009 -> 106182000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	106182000 \|Immune system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (757839021) - 3439009 -> 24484000 (246112005) View
246112005 \|Severity (attribute)\|	24484000 \|Severe (severity modifier) (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (757838029) - 3439009 -> 116003000 (363698007) View
363698007 \|Finding site (attribute)\|	116003000 \|Structure of immune system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (203915029) - 3439009 -> 31323000 (116680003) View
116680003 \|Is a (attribute)\|	31323000 \|Severe combined immunodeficiency disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
31323000 View
31323000	Severe combined immunodeficiency disease (disorder)	Scid	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
111584000 View
111584000	Reticular dysgenesis (disorder)	De vaal disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
190996002 View
190996002	Severe combined immunodeficiency with reticular dysgenesis (disorder)	Severe combined immunodefiency with reticular dysgenesis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (d4370729-7b82-5fe1-bcaf-eca8ca642a25) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D81.1	TRUE	ALWAYS D81.1	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

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