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Terminology chevron_right Concepts chevron_right 766879006

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Component

766879006

The component that hold information about this concept.

Fully Specified Name (FSN)

Combined immunodeficiency due to ox40 deficiency (disorder)

Shortest Term

Combined immunodeficiency due to ox40 deficiency

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

Combined immunodeficiency due to ox40 deficiency (disorder)

SCTID: 766879006, Primitive, Active

766879006|Combined immunodeficiency due to ox40 deficiency (disorder)|

en Combined immunodeficiency due to ox40 deficiency
en Combined immunodeficiency due to ox40 deficiency (disorder)
en Combined immunodeficiency with childhood-onset kaposi sarcoma

Expression

766879006 |Combined immunodeficiency due to ox40 deficiency (disorder)|
 <<< 36138009 |Congenital immunodeficiency disease (disorder)| + 
234632005 |Immunodeficiency associated with chromosomal abnormality (disorder)| + 
414030009 |Disorder of immune structure (disorder)| + 
442459007 |Combined immunodeficiency disease (disorder)| + 
699346009 |Hereditary cancer-predisposing syndrome (disorder)| + 
363138005 |Hereditary disorder of immune system (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 116003000 |Structure of immune system (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 42752001 |Due to (attribute)| = 409709004 |Chromosomal disorder (disorder)| }
        { 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
3662993011 - Combined immunodeficiency due to OX40 deficiency (en) View
3662993011	en	Synonym (core metadata concept)	Combined immunodeficiency due to OX40 deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3662994017 - Combined immunodeficiency due to OX40 deficiency (disorder) (en) View
3662994017	en	Fully specified name (core metadata concept)	Combined immunodeficiency due to OX40 deficiency (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3662996015 - Combined immunodeficiency with childhood-onset Kaposi sarcoma (en) View
3662996015	en	Synonym (core metadata concept)	Combined immunodeficiency with childhood-onset Kaposi sarcoma	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9299140029) - 766879006 -> 409709004 (42752001) View
42752001 \|Due to (attribute)\|	409709004 \|Chromosomal disorder (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11170723025) - 766879006 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9299133025) - 766879006 -> 363138005 (116680003) View
116680003 \|Is a (attribute)\|	363138005 \|Hereditary disorder of immune system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9299134020) - 766879006 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9299135021) - 766879006 -> 414030009 (116680003) View
116680003 \|Is a (attribute)\|	414030009 \|Disorder of immune structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9299136022) - 766879006 -> 442459007 (116680003) View
116680003 \|Is a (attribute)\|	442459007 \|Combined immunodeficiency disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9299137029) - 766879006 -> 699346009 (116680003) View
116680003 \|Is a (attribute)\|	699346009 \|Hereditary cancer-predisposing syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9299138023) - 766879006 -> 116003000 (363698007) View
363698007 \|Finding site (attribute)\|	116003000 \|Structure of immune system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9299139026) - 766879006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9299141025) - 766879006 -> 234632005 (116680003) View
116680003 \|Is a (attribute)\|	234632005 \|Immunodeficiency associated with chromosomal abnormality (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9299142021) - 766879006 -> 36138009 (116680003) View
116680003 \|Is a (attribute)\|	36138009 \|Congenital immunodeficiency disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
699346009 View
699346009	Hereditary cancer-predisposing syndrome (disorder)	Hereditary neoplastic syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
442459007 View
442459007	Combined immunodeficiency disease (disorder)	Combined immunodeficiency disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
414030009 View
414030009	Disorder of immune structure (disorder)	Disorder of immune structure	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
36138009 View
36138009	Congenital immunodeficiency disease (disorder)	Congenital immunodeficiency disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234632005 View
234632005	Immunodeficiency associated with chromosomal abnormality (disorder)	Immunodeficiency associated with chromosomal abnormality	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363138005 View
363138005	Hereditary disorder of immune system (disorder)	Hereditary disorder of immune system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (7f598816-693e-5216-90f6-d4113c7a2bce) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D81.8	TRUE	ALWAYS D81.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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