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Terminology chevron_right Concepts chevron_right 237869003

Production

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Component

237869003

The component that hold information about this concept.

Fully Specified Name (FSN)

Localized hereditary amyloidosis (disorder)

Shortest Term

Localised hereditary amyloidosis

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Localized hereditary amyloidosis (disorder)

SCTID: 237869003, Defined, Active

237869003|Localized hereditary amyloidosis (disorder)|

en Localised hereditary amyloidosis
en Localized hereditary amyloidosis
en Localized hereditary amyloidosis (disorder)
en Organ limited hereditary amyloidosis

Expression

237869003 |Localized hereditary amyloidosis (disorder)|
 === 56871000 |Localized amyloidosis (disorder)| + 
367601000119103 |Hereditary amyloidosis (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 57174000 |Focal amyloid (morphologic abnormality)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
356478017 - Localised hereditary amyloidosis (en) View
356478017	en	Synonym (core metadata concept)	Localised hereditary amyloidosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
356479013 - Localized hereditary amyloidosis (en) View
356479013	en	Synonym (core metadata concept)	Localized hereditary amyloidosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
626660014 - Localized hereditary amyloidosis (disorder) (en) View
626660014	en	Fully specified name (core metadata concept)	Localized hereditary amyloidosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
356477010 - Organ limited hereditary amyloidosis (en) View
356477010	en	Synonym (core metadata concept)	Organ limited hereditary amyloidosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12251930024) - 237869003 -> 367601000119103 (116680003) View
116680003 \|Is a (attribute)\|	367601000119103 \|Hereditary amyloidosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2575218026) - 237869003 -> 57174000 (116676008) View
116676008 \|Associated morphology (attribute)\|	57174000 \|Focal amyloid (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526730020) - 237869003 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526731024) - 237869003 -> 68790008 (116676008) View
116676008 \|Associated morphology (attribute)\|	68790008 \|Amyloid deposition (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53484022) - 237869003 -> 56871000 (116680003) View
116680003 \|Is a (attribute)\|	56871000 \|Localized amyloidosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
367601000119103 View
367601000119103	Hereditary amyloidosis (disorder)	Hereditary amyloidosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
56871000 View
56871000	Localized amyloidosis (disorder)	Localised amyloidosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1187149000 View
1187149000	Localized hereditary amyloidosis of heart (disorder)	Localised hereditary cardiac amyloidosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
361199007 View
361199007	Lattice corneal dystrophy (disorder)	Finland type amyloidosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
724357007 View
724357007	Hereditary cerebral hemorrhage with amyloidosis (disorder)	Hereditary cerebral hemorrhage with amyloidosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237870002 View
237870002	Familial lichen amyloidosis (disorder)	Familial lichen amyloidosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237872005 View
237872005	Poikilodermal cutaneous amyloid (disorder)	Poikilodermal cutaneous amyloid	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (225004eb-4129-5036-a6f2-f7bac7fdf791) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (481bae3c-549b-5fa4-b621-da8aae42b980) 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 (54595af1-db52-5002-b4a7-f18d23b94839) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L99.0	IFA 237871003 \| Papular cutaneous amyloid (disorder) \|	IF PAPULAR CUTANEOUS AMYLOID CHOOSE L99.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (55958141-225c-5c52-98e9-5cee3f9a97b3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	I68.0	IFA 45639009 \| Hereditary cerebral amyloid angiopathy, Icelandic type (disorder) \|	IF HEREDITARY CEREBRAL AMYLOID ANGIOPATHY, ICELANDIC TYPE CHOOSE I68.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (62296bb0-44e0-5d6f-a661-721bfa86ac1a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L99.0	IFA 237872005 \| Poikilodermal cutaneous amyloid (disorder) \|	IF POIKILODERMAL CUTANEOUS AMYLOID CHOOSE L99.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (b214adb3-330e-5769-9177-1047a02ba086) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L99.0	IFA 237870002 \| Familial lichen amyloidosis (disorder) \|	IF FAMILIAL LICHEN AMYLOIDOSIS CHOOSE L99.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (225004eb-4129-5036-a6f2-f7bac7fdf791) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (481bae3c-549b-5fa4-b621-da8aae42b980) 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 (54595af1-db52-5002-b4a7-f18d23b94839) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L99.0	IFA 237871003 \| Papular cutaneous amyloid (disorder) \|	IF PAPULAR CUTANEOUS AMYLOID CHOOSE L99.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (55958141-225c-5c52-98e9-5cee3f9a97b3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	I68.0	IFA 45639009 \| Hereditary cerebral amyloid angiopathy, Icelandic type (disorder) \|	IF HEREDITARY CEREBRAL AMYLOID ANGIOPATHY, ICELANDIC TYPE CHOOSE I68.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (62296bb0-44e0-5d6f-a661-721bfa86ac1a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L99.0	IFA 237872005 \| Poikilodermal cutaneous amyloid (disorder) \|	IF POIKILODERMAL CUTANEOUS AMYLOID CHOOSE L99.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (b214adb3-330e-5769-9177-1047a02ba086) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L99.0	IFA 237870002 \| Familial lichen amyloidosis (disorder) \|	IF FAMILIAL LICHEN AMYLOIDOSIS CHOOSE L99.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

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