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Terminology chevron_right Concepts chevron_right 43532007

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Component

43532007

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary oculoleptomeningeal amyloid angiopathy (disorder)

Shortest Term

Amyloidosis vii

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

Hereditary oculoleptomeningeal amyloid angiopathy (disorder)

SCTID: 43532007, Primitive, Active

43532007|Hereditary oculoleptomeningeal amyloid angiopathy (disorder)|

en Familial oculoleptomeningeal amyloidosis
en Hereditary oculoleptomeningeal amyloid angiopathy
en Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
en Amyloidosis vii
en Ohio type amyloidosis

Expression

43532007 |Hereditary oculoleptomeningeal amyloid angiopathy (disorder)|
 <<< 367601000119103 |Hereditary amyloidosis (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
15758002 |Disorder of meninges (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 68790008 |Amyloid deposition (morphologic abnormality)|,
246075003 |Causative agent (attribute)| = 37959007 |Prealbumin (substance)|,
363698007 |Finding site (attribute)| = 66697007 |Leptomeninges structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
493631014 - Familial oculoleptomeningeal amyloidosis (en) View
493631014	en	Synonym (core metadata concept)	Familial oculoleptomeningeal amyloidosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
72596012 - Hereditary oculoleptomeningeal amyloid angiopathy (en) View
72596012	en	Synonym (core metadata concept)	Hereditary oculoleptomeningeal amyloid angiopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
780556017 - Hereditary oculoleptomeningeal amyloid angiopathy (disorder) (en) View
780556017	en	Fully specified name (core metadata concept)	Hereditary oculoleptomeningeal amyloid angiopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
72597015 - Amyloidosis VII (en) View
72597015	en	Synonym (core metadata concept)	Amyloidosis VII	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
72598013 - Ohio type amyloidosis (en) View
72598013	en	Synonym (core metadata concept)	Ohio type amyloidosis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (218944023) - 43532007 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12490407024) - 43532007 -> 106018006 (116680003) View
116680003 \|Is a (attribute)\|	106018006 \|Hereditary degenerative disease of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (218942022) - 43532007 -> 56871000 (116680003) View
116680003 \|Is a (attribute)\|	56871000 \|Localized amyloidosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (218943028) - 43532007 -> 27550009 (116680003) View
116680003 \|Is a (attribute)\|	27550009 \|Disorder of blood vessel (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (218946020) - 43532007 -> 363005004 (116680003) View
116680003 \|Is a (attribute)\|	363005004 \|Cardiovascular system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (781067029) - 43532007 -> 59820001 (363698007) View
363698007 \|Finding site (attribute)\|	59820001 \|Blood vessel structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2596060021) - 43532007 -> 57174000 (116676008) View
116676008 \|Associated morphology (attribute)\|	57174000 \|Focal amyloid (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12490408025) - 43532007 -> 37959007 (246075003) View
246075003 \|Causative agent (attribute)\|	37959007 \|Prealbumin (substance)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12490409022) - 43532007 -> 68790008 (116676008) View
116676008 \|Associated morphology (attribute)\|	68790008 \|Amyloid deposition (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (781069026) - 43532007 -> 66697007 (363698007) View
363698007 \|Finding site (attribute)\|	66697007 \|Leptomeninges structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7115688027) - 43532007 -> 367601000119103 (116680003) View
116680003 \|Is a (attribute)\|	367601000119103 \|Hereditary amyloidosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (781068023) - 43532007 -> 68790008 (116676008) View
116676008 \|Associated morphology (attribute)\|	68790008 \|Amyloid deposition (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (218945024) - 43532007 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (218947027) - 43532007 -> 15758002 (116680003) View
116680003 \|Is a (attribute)\|	15758002 \|Disorder of meninges (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
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
15758002 View
15758002	Disorder of meninges (disorder)	Disorder of meninges	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363235000 View
363235000	Hereditary disorder of nervous system (disorder)	Hereditary disorder of nervous system	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 (8f5c7ddb-6fd2-5dae-bbf0-87156598e4fd) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E85.1	TRUE	ALWAYS E85.1	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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