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Terminology chevron_right Concepts chevron_right 402614008

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Component

402614008

The component that hold information about this concept.

Fully Specified Name (FSN)

Hypermelanosis due to connective tissue disorder (disorder)

Shortest Term

Hypermelanosis due to connective tissue disorder

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 due to connective tissue disorder (disorder)

SCTID: 402614008, Defined, Active

402614008|Hypermelanosis due to connective tissue disorder (disorder)|

en Hypermelanosis due to connective tissue disorder
en Hypermelanosis due to connective tissue disorder (disorder)

Expression

402614008 |Hypermelanosis due to connective tissue disorder (disorder)|
 === 238698004 |Acquired hypermelanotic disorder (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)| }
        { 42752001 |Due to (attribute)| = 105969002 |Disorder of connective tissue (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1781728013 - Hypermelanosis due to connective tissue disorder (en) View
1781728013	en	Synonym (core metadata concept)	Hypermelanosis due to connective tissue disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1770538016 - Hypermelanosis due to connective tissue disorder (disorder) (en) View
1770538016	en	Fully specified name (core metadata concept)	Hypermelanosis due to connective tissue disorder (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2640611023) - 402614008 -> 105969002 (42752001) View
42752001 \|Due to (attribute)\|	105969002 \|Disorder of connective tissue (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2755095024) - 402614008 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9334853027) - 402614008 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9334854022) - 402614008 -> 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 (9334855023) - 402614008 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2287760028) - 402614008 -> 4830009 (116676008) View
116676008 \|Associated morphology (attribute)\|	4830009 \|Hyperpigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2287762020) - 402614008 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2287761029) - 402614008 -> 105969002 (363715002) View
363715002 \|Associated etiologic finding (attribute)\|	105969002 \|Disorder of connective tissue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2248740024) - 402614008 -> 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

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
403507009 View
403507009	Lupus erythematosus-associated hypermelanosis (disorder)	Hypermelanosis due to lupus erythematosus	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
403515007 View
403515007	Scleroderma-associated hypermelanosis (disorder)	Scleroderma-associated hypermelanosis	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 (147a0b10-1114-5d14-b874-344e52a16647) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	M35.8	TRUE	ALWAYS M35.8	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 (fa409279-5e43-597f-b37a-6332ca4e96f0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L81.4	TRUE	ALWAYS L81.4 \| 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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