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Terminology chevron_right Concepts chevron_right 201285006

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Component

201285006

The component that hold information about this concept.

Fully Specified Name (FSN)

Lentigo - freckle (disorder)

Shortest Term

Lentigo - freckle

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

Lentigo - freckle (disorder)

SCTID: 201285006, Primitive, Active

201285006|Lentigo - freckle (disorder)|

en Lentigo - freckle
en Lentigo - freckle (disorder)

Expression

201285006 |Lentigo - freckle (disorder)|
 <<< 46690002 |Disorder of skin pigmentation (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 79644001 |Pigment alteration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
309222011 - Lentigo - freckle (en) View
309222011	en	Synonym (core metadata concept)	Lentigo - freckle	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
586139014 - Lentigo - freckle (disorder) (en) View
586139014	en	Fully specified name (core metadata concept)	Lentigo - freckle (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (1938128021) - 201285006 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2743137020) - 201285006 -> 79644001 (116676008) View
116676008 \|Associated morphology (attribute)\|	79644001 \|Pigment alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3345254027) - 201285006 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3345255026) - 201285006 -> 79644001 (116676008) View
116676008 \|Associated morphology (attribute)\|	79644001 \|Pigment alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (966711023) - 201285006 -> 51083003 (116676008) View
116676008 \|Associated morphology (attribute)\|	51083003 \|Structure showing abnormal deposition of pigment (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (966712027) - 201285006 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (329456021) - 201285006 -> 239129006 (116680003) View
116680003 \|Is a (attribute)\|	239129006 \|Miscellaneous disorders of skin pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1693921027) - 201285006 -> 46690002 (116680003) View
116680003 \|Is a (attribute)\|	46690002 \|Disorder of skin pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
46690002 View
46690002	Disorder of skin pigmentation (disorder)	Dyschromia	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 (326fd609-114e-5ee4-90c7-658a6eb3ab77) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	SOURCE SNOMED CONCEPT IS AMBIGUOUS	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447640006 \|Source snomed concept is ambiguous (foundation metadata concept)\|

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