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Terminology chevron_right Concepts chevron_right 403515007

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Component

403515007

The component that hold information about this concept.

Fully Specified Name (FSN)

Scleroderma-associated hypermelanosis (disorder)

Shortest Term

Scleroderma-associated hypermelanosis

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

Scleroderma-associated hypermelanosis (disorder)

SCTID: 403515007, Defined, Active

403515007|Scleroderma-associated hypermelanosis (disorder)|

en Hypermelanosis due to systemic sclerosis
en Scleroderma-associated hypermelanosis
en Scleroderma-associated hypermelanosis (disorder)

Expression

403515007 |Scleroderma-associated hypermelanosis (disorder)|
 === 402614008 |Hypermelanosis due to connective tissue disorder (disorder)| + 
402713007 |Cutaneous complication of systemic sclerosis (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)| = 89155008 |Systemic sclerosis (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1787784015 - Hypermelanosis due to systemic sclerosis (en) View
1787784015	en	Synonym (core metadata concept)	Hypermelanosis due to systemic sclerosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1782550010 - Scleroderma-associated hypermelanosis (en) View
1782550010	en	Synonym (core metadata concept)	Scleroderma-associated hypermelanosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1771441016 - Scleroderma-associated hypermelanosis (disorder) (en) View
1771441016	en	Fully specified name (core metadata concept)	Scleroderma-associated hypermelanosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2641019029) - 403515007 -> 105969002 (42752001) View
42752001 \|Due to (attribute)\|	105969002 \|Disorder of connective tissue (disorder)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2755455027) - 403515007 -> 89155008 (47429007) View
47429007 \|Associated with (attribute)\|	89155008 \|Systemic sclerosis (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12378744027) - 403515007 -> 89155008 (42752001) View
42752001 \|Due to (attribute)\|	89155008 \|Systemic sclerosis (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2776789023) - 403515007 -> 46690002 (116680003) View
116680003 \|Is a (attribute)\|	46690002 \|Disorder of skin pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9335326028) - 403515007 -> 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 (2755456026) - 403515007 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2798182021) - 403515007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3420146029) - 403515007 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3461591022) - 403515007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2755454028) - 403515007 -> 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 (2290225021) - 403515007 -> 84820005 (363698007) View
363698007 \|Finding site (attribute)\|	84820005 \|Structure of fascia (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2290226022) - 403515007 -> 43846000 (116676008) View
116676008 \|Associated morphology (attribute)\|	43846000 \|Sclerosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2290228023) - 403515007 -> 4830009 (116676008) View
116676008 \|Associated morphology (attribute)\|	4830009 \|Hyperpigmentation (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2290229026) - 403515007 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2290227029) - 403515007 -> 105969002 (363715002) View
363715002 \|Associated etiologic finding (attribute)\|	105969002 \|Disorder of connective tissue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2250051022) - 403515007 -> 402614008 (116680003) View
116680003 \|Is a (attribute)\|	402614008 \|Hypermelanosis due to connective tissue disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2250052026) - 403515007 -> 402713007 (116680003) View
116680003 \|Is a (attribute)\|	402713007 \|Cutaneous complication of systemic sclerosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
402713007 View
402713007	Cutaneous complication of systemic sclerosis (disorder)	Cutaneous complication of systemic sclerosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
402614008 View
402614008	Hypermelanosis due to connective tissue disorder (disorder)	Hypermelanosis due to connective tissue 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 (69fab434-89b7-5e39-b182-a880066162d2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	M34.9	TRUE	ALWAYS M34.9	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 (d1d86f8c-6996-5639-9e7f-9c3d8eec1f03) 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)\|
ExtendedMap object (df076500-6dd5-5fb5-b2bf-4563ddd125fe) 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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