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Terminology chevron_right Concepts chevron_right 403539002

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Component

403539002

The component that hold information about this concept.

Fully Specified Name (FSN)

Zosteriform lentiginosis (disorder)

Shortest Term

Zosteriform lentiginosis

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

Zosteriform lentiginosis (disorder)

SCTID: 403539002, Primitive, Active

403539002|Zosteriform lentiginosis (disorder)|

en Zosteriform lentiginosis
en Zosteriform lentiginosis (disorder)

Expression

403539002 |Zosteriform lentiginosis (disorder)|
 <<< 399921006 |Hamartoma of skin (disorder)| + 
402624000 |Lentiginosis (disorder)| + 
49765009 |Hyperpigmentation of skin (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 767376003 |Lentigo (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1782566012 - Zosteriform lentiginosis (en) View
1782566012	en	Synonym (core metadata concept)	Zosteriform lentiginosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1771465018 - Zosteriform lentiginosis (disorder) (en) View
1771465018	en	Fully specified name (core metadata concept)	Zosteriform lentiginosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9358774020) - 403539002 -> 239086004 (116680003) View
116680003 \|Is a (attribute)\|	239086004 \|Zosteriform reticulate hyperpigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12251940022) - 403539002 -> 49765009 (116680003) View
116680003 \|Is a (attribute)\|	49765009 \|Hyperpigmentation of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2250084022) - 403539002 -> 403538005 (116680003) View
116680003 \|Is a (attribute)\|	403538005 \|Nevoid lentiginosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3413754020) - 403539002 -> 41162001 (116676008) View
116676008 \|Associated morphology (attribute)\|	41162001 \|Increased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9358773025) - 403539002 -> 399921006 (116680003) View
116680003 \|Is a (attribute)\|	399921006 \|Hamartoma of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9358775021) - 403539002 -> 402624000 (116680003) View
116680003 \|Is a (attribute)\|	402624000 \|Lentiginosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9358776022) - 403539002 -> 767376003 (116676008) View
116676008 \|Associated morphology (attribute)\|	767376003 \|Lentigo (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2290288021) - 403539002 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2798187026) - 403539002 -> 41162001 (116676008) View
116676008 \|Associated morphology (attribute)\|	41162001 \|Increased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3413755021) - 403539002 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2641025025) - 403539002 -> 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 (2641026029) - 403539002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
49765009 View
49765009	Hyperpigmentation of skin (disorder)	Tăng sắc tố da	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
402624000 View
402624000	Lentiginosis (disorder)	Tàn nhang	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
399921006 View
399921006	Hamartoma of skin (disorder)	Hamartoma of skin	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 (0c3f915a-374d-5273-87c2-cd305a54d1df) 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 (fa76117b-9e54-59d3-80cc-838b4e81e113) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D23.9	TRUE	ALWAYS D23.9 \| POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE	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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