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Terminology chevron_right Concepts chevron_right 1717003

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Component

1717003

The component that hold information about this concept.

Fully Specified Name (FSN)

Idiopathic guttate hypomelanosis (disorder)

Shortest Term

Guttate hypomelanosis

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

Idiopathic guttate hypomelanosis (disorder)

SCTID: 1717003, Primitive, Active

1717003|Idiopathic guttate hypomelanosis (disorder)|

en Guttate hypomelanosis
en Idiopathic guttate hypomelanosis
en Idiopathic guttate hypomelanosis (disorder)

Expression

1717003 |Idiopathic guttate hypomelanosis (disorder)|
 <<< 403276003 |Acquired hypomelanosis of uncertain etiology (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
3036349016 - Guttate hypomelanosis (en) View
3036349016	en	Synonym (core metadata concept)	Guttate hypomelanosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3969010 - Idiopathic guttate hypomelanosis (en) View
3969010	en	Synonym (core metadata concept)	Idiopathic guttate hypomelanosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
744337017 - Idiopathic guttate hypomelanosis (disorder) (en) View
744337017	en	Fully specified name (core metadata concept)	Idiopathic guttate hypomelanosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12489522021) - 1717003 -> 41969006 (116680003) View
116680003 \|Is a (attribute)\|	41969006 \|Idiopathic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (712686027) - 1717003 -> 18655006 (116676008) View
116676008 \|Associated morphology (attribute)\|	18655006 \|Depigmentation (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9502691020) - 1717003 -> 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 (1927762023) - 1717003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2591552025) - 1717003 -> 37257004 (116676008) View
116676008 \|Associated morphology (attribute)\|	37257004 \|Decreased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3355529024) - 1717003 -> 37257004 (116676008) View
116676008 \|Associated morphology (attribute)\|	37257004 \|Decreased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3455773022) - 1717003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (712687020) - 1717003 -> 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 (2264678028) - 1717003 -> 89031001 (116676008) View
116676008 \|Associated morphology (attribute)\|	89031001 \|Hypopigmentation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (174088023) - 1717003 -> 46690002 (116680003) View
116680003 \|Is a (attribute)\|	46690002 \|Disorder of skin pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2225484027) - 1717003 -> 403276003 (116680003) View
116680003 \|Is a (attribute)\|	403276003 \|Acquired hypomelanosis of uncertain etiology (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (712688026) - 1717003 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
403276003 View
403276003	Acquired hypomelanosis of uncertain etiology (disorder)	Acquired idiopathic hypomelanosis	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 (38d3179d-b093-5bcc-8452-e93eadbf30f2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L81.5	TRUE	ALWAYS L81.5	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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