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Terminology chevron_right Concepts chevron_right 1186715006

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Component

1186715006

The component that hold information about this concept.

Fully Specified Name (FSN)

Combined immunodeficiency due to cd70 deficiency (disorder)

Shortest Term

Combined immunodeficiency due to cd70 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 cd70 deficiency (disorder)

SCTID: 1186715006, Primitive, Active

1186715006|Combined immunodeficiency due to cd70 deficiency (disorder)|

en Combined immunodeficiency due to cd70 deficiency
en Combined immunodeficiency due to cd70 deficiency (disorder)

Expression

1186715006 |Combined immunodeficiency due to cd70 deficiency (disorder)|
 <<< 277466009 |Lymphoproliferative disorder (disorder)| + 
442459007 |Combined immunodeficiency disease (disorder)| + 
699346009 |Hereditary cancer-predisposing syndrome (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 414629003 |Lymphoproliferative disorder (morphologic abnormality)| }
        { 370135005 |Pathological process (attribute)| = 769256002 |Dysregulated host response (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4667416014 - Combined immunodeficiency due to CD70 deficiency (en) View
4667416014	en	Synonym (core metadata concept)	Combined immunodeficiency due to CD70 deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
4667415013 - Combined immunodeficiency due to CD70 deficiency (disorder) (en) View
4667415013	en	Fully specified name (core metadata concept)	Combined immunodeficiency due to CD70 deficiency (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (14956471023) - 1186715006 -> 277466009 (116680003) View
116680003 \|Is a (attribute)\|	277466009 \|Lymphoproliferative disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14956472027) - 1186715006 -> 442459007 (116680003) View
116680003 \|Is a (attribute)\|	442459007 \|Combined immunodeficiency disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14956473021) - 1186715006 -> 699346009 (116680003) View
116680003 \|Is a (attribute)\|	699346009 \|Hereditary cancer-predisposing syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14956474026) - 1186715006 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14956475025) - 1186715006 -> 414629003 (116676008) View
116676008 \|Associated morphology (attribute)\|	414629003 \|Lymphoproliferative disorder (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14956513028) - 1186715006 -> 769256002 (370135005) View
370135005 \|Pathological process (attribute)\|	769256002 \|Dysregulated host response (qualifier value)\|	2	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
277466009 View
277466009	Lymphoproliferative disorder (disorder)	Bệnh tăng sinh mô bạch huyết	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

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 (ec6ad01b-5e03-539e-ad67-c8343afa34c5) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D82.3	TRUE	ALWAYS D82.3 \| 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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