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Terminology chevron_right Concepts chevron_right 402806000

Production

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Component

402806000

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital/hereditary lentiginosis (disorder)

Shortest Term

Congenital/hereditary 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

Congenital/hereditary lentiginosis (disorder)

SCTID: 402806000, Primitive, Inactive

402806000|Congenital/hereditary lentiginosis (disorder)|

en Congenital/hereditary lentiginosis
en Congenital/hereditary lentiginosis (disorder)

Expression

402806000 |Congenital/hereditary lentiginosis (disorder)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1781898014 - Congenital/hereditary lentiginosis (en) View
1781898014	en	Synonym (core metadata concept)	Congenital/hereditary lentiginosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1770730013 - Congenital/hereditary lentiginosis (disorder) (en) View
1770730013	en	Fully specified name (core metadata concept)	Congenital/hereditary lentiginosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2248978025) - 402806000 -> 402624000 (116680003) View
116680003 \|Is a (attribute)\|	402624000 \|Lentiginosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3375999023) - 402806000 -> 41162001 (116676008) View
116676008 \|Associated morphology (attribute)\|	41162001 \|Increased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3376000020) - 402806000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2288184025) - 402806000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2797927025) - 402806000 -> 41162001 (116676008) View
116676008 \|Associated morphology (attribute)\|	41162001 \|Increased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2640698029) - 402806000 -> 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 (2565377029) - 402806000 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2640699021) - 402806000 -> 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

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 (283aee1b-87bc-5d8e-b8ca-46d12f46cd1b) 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)\|

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2248978025) - 402806000 -> 402624000 (116680003) View
116680003 \|Is a (attribute)\|	402624000 \|Lentiginosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3375999023) - 402806000 -> 41162001 (116676008) View
116676008 \|Associated morphology (attribute)\|	41162001 \|Increased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3376000020) - 402806000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2288184025) - 402806000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2797927025) - 402806000 -> 41162001 (116676008) View
116676008 \|Associated morphology (attribute)\|	41162001 \|Increased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2640698029) - 402806000 -> 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 (2565377029) - 402806000 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2640699021) - 402806000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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