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Terminology chevron_right Concepts chevron_right 95370008

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Component

95370008

The component that hold information about this concept.

Fully Specified Name (FSN)

Application site pigmentation changes (disorder)

Shortest Term

Application site pigmentation changes

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

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

Summary

Application site pigmentation changes (disorder)

SCTID: 95370008, Defined, Active

95370008|Application site pigmentation changes (disorder)|

en Application site pigmentation changes
en Application site pigmentation changes (disorder)

Expression

95370008 |Application site pigmentation changes (disorder)|
 === 95364002 |Application site disorder (disorder)| + 
414032001 |Disorder of pigmentation (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 79644001 |Pigment alteration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39801007 |Application site (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
157997018 - Application site pigmentation changes (en) View
157997018	en	Synonym (core metadata concept)	Application site pigmentation changes	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
839509012 - Application site pigmentation changes (disorder) (en) View
839509012	en	Fully specified name (core metadata concept)	Application site pigmentation changes (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (7389696024) - 95370008 -> 71388002 (42752001) View
42752001 \|Due to (attribute)\|	71388002 \|Procedure (procedure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3236211027) - 95370008 -> 71388002 (47429007) View
47429007 \|Associated with (attribute)\|	71388002 \|Procedure (procedure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2604836022) - 95370008 -> 79644001 (116676008) View
116676008 \|Associated morphology (attribute)\|	79644001 \|Pigment alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2604837029) - 95370008 -> 39801007 (363698007) View
363698007 \|Finding site (attribute)\|	39801007 \|Application site (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3350465029) - 95370008 -> 39801007 (363698007) View
363698007 \|Finding site (attribute)\|	39801007 \|Application site (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3350466028) - 95370008 -> 79644001 (116676008) View
116676008 \|Associated morphology (attribute)\|	79644001 \|Pigment alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2604835021) - 95370008 -> 71388002 (255234002) View
255234002 \|After (attribute)\|	71388002 \|Procedure (procedure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2699151026) - 95370008 -> 414032001 (116680003) View
116680003 \|Is a (attribute)\|	414032001 \|Disorder of pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (929177022) - 95370008 -> 71388002 (363708005) View
363708005 \|Temporally follows (attribute)\|	71388002 \|Procedure (procedure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (929178028) - 95370008 -> 51083003 (116676008) View
116676008 \|Associated morphology (attribute)\|	51083003 \|Structure showing abnormal deposition of pigment (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2050599027) - 95370008 -> 127856007 (363698007) View
363698007 \|Finding site (attribute)\|	127856007 \|Skin and/or subcutaneous tissue structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (929176029) - 95370008 -> 39801007 (363698007) View
363698007 \|Finding site (attribute)\|	39801007 \|Application site (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (307033022) - 95370008 -> 95364002 (116680003) View
116680003 \|Is a (attribute)\|	95364002 \|Application site disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
414032001 View
414032001	Disorder of pigmentation (disorder)	Disorder of pigmentation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
95364002 View
95364002	Application site disorder (disorder)	Application site disorder	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 (82c5c3b1-0bb1-5772-873c-24dce5014101) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L81.9	TRUE	ALWAYS L81.9	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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