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Terminology chevron_right Concepts chevron_right 403260007

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Component

403260007

The component that hold information about this concept.

Fully Specified Name (FSN)

Hypermelanosis of undetermined etiology (disorder)

Shortest Term

Hypermelanosis of undetermined etiology

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

Hypermelanosis of undetermined etiology (disorder)

SCTID: 403260007, Defined, Active

403260007|Hypermelanosis of undetermined etiology (disorder)|

en Hypermelanosis of undetermined aetiology
en Hypermelanosis of undetermined etiology
en Hypermelanosis of undetermined etiology (disorder)

Expression

403260007 |Hypermelanosis of undetermined etiology (disorder)|
 === 238698004 |Acquired hypermelanotic disorder (disorder)| + 
41969006 |Idiopathic disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 48010006 |Melanosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)|,
246454002 |Occurrence (attribute)| = 767023003 |Period of life beginning after birth and ending before death (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1773703019 - Hypermelanosis of undetermined aetiology (en) View
1773703019	en	Synonym (core metadata concept)	Hypermelanosis of undetermined aetiology	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1774989015 - Hypermelanosis of undetermined etiology (en) View
1774989015	en	Synonym (core metadata concept)	Hypermelanosis of undetermined etiology	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1771186010 - Hypermelanosis of undetermined etiology (disorder) (en) View
1771186010	en	Fully specified name (core metadata concept)	Hypermelanosis of undetermined etiology (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15669892021) - 403260007 -> 41969006 (116680003) View
116680003 \|Is a (attribute)\|	41969006 \|Idiopathic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2755334025) - 403260007 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9334750022) - 403260007 -> 767023003 (246454002) View
246454002 \|Occurrence (attribute)\|	767023003 \|Period of life beginning after birth and ending before death (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9334751021) - 403260007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9334752025) - 403260007 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2289467023) - 403260007 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2289468029) - 403260007 -> 4830009 (116676008) View
116676008 \|Associated morphology (attribute)\|	4830009 \|Hyperpigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2249704027) - 403260007 -> 238698004 (116680003) View
116680003 \|Is a (attribute)\|	238698004 \|Acquired hypermelanotic disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
238698004 View
238698004	Acquired hypermelanotic disorder (disorder)	Acquired hypermelanotic disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
41969006 View
41969006	Idiopathic disease (disorder)	Idiopathic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
79840007 View
79840007	Idiopathic chloasma (disorder)	Idiopathic chloasma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (1c9b57a1-df32-5c30-8726-a943d10f9085) 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)\|
ExtendedMap object (9e46e6ed-668d-5f23-a3c0-852960c12928) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L81.4	TRUE	ALWAYS L81.4	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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