dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 403276003

Production

add

Component

403276003

The component that hold information about this concept.

Fully Specified Name (FSN)

Acquired hypomelanosis of uncertain etiology (disorder)

Shortest Term

Acquired idiopathic hypomelanosis

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

Acquired hypomelanosis of uncertain etiology (disorder)

SCTID: 403276003, Defined, Active

403276003|Acquired hypomelanosis of uncertain etiology (disorder)|

en Acquired idiopathic hypomelanosis
en Acquired hypomelanosis of uncertain aetiology
en Acquired hypomelanosis of uncertain etiology
en Acquired hypomelanosis of uncertain etiology (disorder)

Expression

403276003 |Acquired hypomelanosis of uncertain etiology (disorder)|
 === 398656003 |Acquired hypomelanotic disorder (disorder)| + 
41969006 |Idiopathic disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 37257004 |Decreased melanin pigmentation (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
4554789015 - Acquired idiopathic hypomelanosis (en) View
4554789015	en	Synonym (core metadata concept)	Acquired idiopathic hypomelanosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1773709015 - Acquired hypomelanosis of uncertain aetiology (en) View
1773709015	en	Synonym (core metadata concept)	Acquired hypomelanosis of uncertain aetiology	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1774995019 - Acquired hypomelanosis of uncertain etiology (en) View
1774995019	en	Synonym (core metadata concept)	Acquired hypomelanosis of uncertain etiology	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1771202015 - Acquired hypomelanosis of uncertain etiology (disorder) (en) View
1771202015	en	Fully specified name (core metadata concept)	Acquired hypomelanosis of uncertain etiology (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13751703026) - 403276003 -> 41969006 (116680003) View
116680003 \|Is a (attribute)\|	41969006 \|Idiopathic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9501892029) - 403276003 -> 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 (2289507024) - 403276003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2640898026) - 403276003 -> 37257004 (116676008) View
116676008 \|Associated morphology (attribute)\|	37257004 \|Decreased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3397581028) - 403276003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3454120021) - 403276003 -> 37257004 (116676008) View
116676008 \|Associated morphology (attribute)\|	37257004 \|Decreased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2289505027) - 403276003 -> 89031001 (116676008) View
116676008 \|Associated morphology (attribute)\|	89031001 \|Hypopigmentation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2289506026) - 403276003 -> 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 (2249722029) - 403276003 -> 398656003 (116680003) View
116680003 \|Is a (attribute)\|	398656003 \|Acquired hypomelanotic disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
398656003 View
398656003	Acquired hypomelanotic disorder (disorder)	Acquired hypomelanosis	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
403275004 View
403275004	Alezzandrini syndrome (disorder)	Alezzandrini syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
403337001 View
403337001	Poliosis in vogt-koyanagi-harada syndrome (disorder)	Poliosis in vogt-koyanagi-harada syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1717003 View
1717003	Idiopathic guttate hypomelanosis (disorder)	Guttate hypomelanosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
239083007 View
239083007	Symmetrical progressive leucopathy (disorder)	Symmetrical progressive leucopathy	900000000000074008 \|Necessary but not sufficient concept 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 (229dc951-2c23-555b-af64-e0c9f9892129) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L81.6	TRUE	ALWAYS L81.6	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)\|

Terminology chevron_right Concepts chevron_right 403276003

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches