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Terminology chevron_right Concepts chevron_right 1197482007

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Component

1197482007

The component that hold information about this concept.

Fully Specified Name (FSN)

Susceptibility to localized juvenile periodontitis (disorder)

Shortest Term

Susceptibility to localised juvenile periodontitis

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

Susceptibility to localized juvenile periodontitis (disorder)

SCTID: 1197482007, Primitive, Active

1197482007|Susceptibility to localized juvenile periodontitis (disorder)|

en Susceptibility to localised juvenile periodontitis
en Susceptibility to localized juvenile periodontitis
en Susceptibility to localized juvenile periodontitis (disorder)

Expression

1197482007 |Susceptibility to localized juvenile periodontitis (disorder)|
 <<< 402794002 |Heritable disorder of neutrophil function (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
1197483002 |Functional disorder of polymorphonuclear neutrophil (disorder)| + 
234580003 |Defective phagocytic cell chemotaxis (disorder)| : 
        { 363698007 |Finding site (attribute)| = 116003000 |Structure of immune system (body structure)|,
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
4696520012 - Susceptibility to localised juvenile periodontitis (en) View
4696520012	en	Synonym (core metadata concept)	Susceptibility to localised juvenile periodontitis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4696518014 - Susceptibility to localized juvenile periodontitis (en) View
4696518014	en	Synonym (core metadata concept)	Susceptibility to localized juvenile periodontitis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4696519018 - Susceptibility to localized juvenile periodontitis (disorder) (en) View
4696519018	en	Fully specified name (core metadata concept)	Susceptibility to localized juvenile periodontitis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15030674021) - 1197482007 -> 402794002 (116680003) View
116680003 \|Is a (attribute)\|	402794002 \|Heritable disorder of neutrophil function (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15030676023) - 1197482007 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15030677025) - 1197482007 -> 116003000 (363698007) View
363698007 \|Finding site (attribute)\|	116003000 \|Structure of immune system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15030678024) - 1197482007 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15030685023) - 1197482007 -> 1197483002 (116680003) View
116680003 \|Is a (attribute)\|	1197483002 \|Functional disorder of polymorphonuclear neutrophil (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15030687026) - 1197482007 -> 234580003 (116680003) View
116680003 \|Is a (attribute)\|	234580003 \|Defective phagocytic cell chemotaxis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1197483002 View
1197483002	Functional disorder of polymorphonuclear neutrophil (disorder)	Functional disorder of polymorphonuclear neutrophil	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
402794002 View
402794002	Heritable disorder of neutrophil function (disorder)	Heritable disorder of neutrophil function	900000000000074008 \|Necessary but not sufficient concept 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
234580003 View
234580003	Defective phagocytic cell chemotaxis (disorder)	Defective phagocytic cell chemotaxis	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 (182f97a3-392f-58e4-83a9-384cda8dde6d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D71	TRUE	ALWAYS D71 \| 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)\|

Terminology chevron_right Concepts chevron_right 1197482007

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