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Terminology chevron_right Concepts chevron_right 237870002

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Component

237870002

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial lichen amyloidosis (disorder)

Shortest Term

Familial lichen amyloidosis

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

Familial lichen amyloidosis (disorder)

SCTID: 237870002, Primitive, Active

237870002|Familial lichen amyloidosis (disorder)|

en Familial lichen amyloidosis
en Familial lichen amyloidosis (disorder)

Expression

237870002 |Familial lichen amyloidosis (disorder)|
 <<< 237869003 |Localized hereditary amyloidosis (disorder)| + 
201337008 |Amyloidosis of skin (disorder)| + 
363185004 |Hereditary disorder of the integument (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 57174000 |Focal amyloid (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
356480011 - Familial lichen amyloidosis (en) View
356480011	en	Synonym (core metadata concept)	Familial lichen amyloidosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
626661013 - Familial lichen amyloidosis (disorder) (en) View
626661013	en	Fully specified name (core metadata concept)	Familial lichen amyloidosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12490410028) - 237870002 -> 201337008 (116680003) View
116680003 \|Is a (attribute)\|	201337008 \|Amyloidosis of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12490411029) - 237870002 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12490412020) - 237870002 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2575219023) - 237870002 -> 57174000 (116676008) View
116676008 \|Associated morphology (attribute)\|	57174000 \|Focal amyloid (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526732028) - 237870002 -> 68790008 (116676008) View
116676008 \|Associated morphology (attribute)\|	68790008 \|Amyloid deposition (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526733022) - 237870002 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53485023) - 237870002 -> 237869003 (116680003) View
116680003 \|Is a (attribute)\|	237869003 \|Localized hereditary amyloidosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
237869003 View
237869003	Localized hereditary amyloidosis (disorder)	Localised hereditary amyloidosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
201337008 View
201337008	Amyloidosis of skin (disorder)	Amyloidosis of skin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363185004 View
363185004	Hereditary disorder of the integument (disorder)	Hereditary disorder of the integument	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 (559da282-815c-56bc-954c-14b05225181b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E85.4	TRUE	ALWAYS E85.4	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 (d7ecc05a-f632-59de-831d-82944c545554) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L99.0	TRUE	ALWAYS L99.0 \| THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE	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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