dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 237872005

Production

add

Component

237872005

The component that hold information about this concept.

Fully Specified Name (FSN)

Poikilodermal cutaneous amyloid (disorder)

Shortest Term

Poikilodermal cutaneous amyloid

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

Poikilodermal cutaneous amyloid (disorder)

SCTID: 237872005, Primitive, Active

237872005|Poikilodermal cutaneous amyloid (disorder)|

en Poikilodermal cutaneous amyloid
en Poikilodermal cutaneous amyloid (disorder)

Expression

237872005 |Poikilodermal cutaneous amyloid (disorder)|
 <<< 201337008 |Amyloidosis of skin (disorder)| + 
237869003 |Localized hereditary amyloidosis (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
356482015 - Poikilodermal cutaneous amyloid (en) View
356482015	en	Synonym (core metadata concept)	Poikilodermal cutaneous amyloid	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
626663011 - Poikilodermal cutaneous amyloid (disorder) (en) View
626663011	en	Fully specified name (core metadata concept)	Poikilodermal cutaneous amyloid (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12251932027) - 237872005 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526736025) - 237872005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2575221029) - 237872005 -> 57174000 (116676008) View
116676008 \|Associated morphology (attribute)\|	57174000 \|Focal amyloid (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3308393024) - 237872005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3440139028) - 237872005 -> 57174000 (116676008) View
116676008 \|Associated morphology (attribute)\|	57174000 \|Focal amyloid (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526737023) - 237872005 -> 68790008 (116676008) View
116676008 \|Associated morphology (attribute)\|	68790008 \|Amyloid deposition (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53488020) - 237872005 -> 201337008 (116680003) View
116680003 \|Is a (attribute)\|	201337008 \|Amyloidosis of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (53489028) - 237872005 -> 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 (5fab90f3-b5b0-55d0-ab5e-160f7f9c8f5c) 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)\|
ExtendedMap object (7a1cce46-6ba1-5e71-9237-0fd848272800) 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)\|

Terminology chevron_right Concepts chevron_right 237872005

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches