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Terminology chevron_right Concepts chevron_right 733422008

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Component

733422008

The component that hold information about this concept.

Fully Specified Name (FSN)

Prion protein systemic amyloidosis (disorder)

Shortest Term

Prion protein systemic 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

Prion protein systemic amyloidosis (disorder)

SCTID: 733422008, Primitive, Active

733422008|Prion protein systemic amyloidosis (disorder)|

en Chronic diarrhea with hereditary sensory and autonomic neuropathy
en Chronic diarrhoea with hereditary sensory and autonomic neuropathy
en Prion protein systemic amyloidosis
en Prion protein systemic amyloidosis (disorder)
en Prp (prion protein) systemic amyloidosis

Expression

733422008 |Prion protein systemic amyloidosis (disorder)|
 <<< 89449005 |Systemic amyloidosis (disorder)| + 
367601000119103 |Hereditary amyloidosis (disorder)| + 
106018006 |Hereditary degenerative disease of central nervous system (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
20484008 |Prion disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 68790008 |Amyloid deposition (morphologic abnormality)| }
        { 116676008 |Associated morphology (attribute)| = 68245003 |Spongy degeneration (morphologic abnormality)|,
246075003 |Causative agent (attribute)| = 84676004 |Prion (organism)|,
363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)|,
370135005 |Pathological process (attribute)| = 441862004 |Infectious process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3499407011 - Chronic diarrhea with hereditary sensory and autonomic neuropathy (en) View
3499407011	en	Synonym (core metadata concept)	Chronic diarrhea with hereditary sensory and autonomic neuropathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3499404016 - Chronic diarrhoea with hereditary sensory and autonomic neuropathy (en) View
3499404016	en	Synonym (core metadata concept)	Chronic diarrhoea with hereditary sensory and autonomic neuropathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3499405015 - Prion protein systemic amyloidosis (en) View
3499405015	en	Synonym (core metadata concept)	Prion protein systemic amyloidosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3499403010 - Prion protein systemic amyloidosis (disorder) (en) View
3499403010	en	Fully specified name (core metadata concept)	Prion protein systemic amyloidosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3499406019 - PrP (prion protein) systemic amyloidosis (en) View
3499406019	en	Synonym (core metadata concept)	PrP (prion protein) systemic amyloidosis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (7008577022) - 733422008 -> 280369009 (363698007) View
363698007 \|Finding site (attribute)\|	280369009 \|Brain tissue structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15805486024) - 733422008 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7008574026) - 733422008 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12093016025) - 733422008 -> 106018006 (116680003) View
116680003 \|Is a (attribute)\|	106018006 \|Hereditary degenerative disease of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7008570024) - 733422008 -> 68790008 (116676008) View
116676008 \|Associated morphology (attribute)\|	68790008 \|Amyloid deposition (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7008571023) - 733422008 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7008572027) - 733422008 -> 20484008 (116680003) View
116680003 \|Is a (attribute)\|	20484008 \|Prion disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7008573021) - 733422008 -> 89449005 (116680003) View
116680003 \|Is a (attribute)\|	89449005 \|Systemic amyloidosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7008575025) - 733422008 -> 68245003 (116676008) View
116676008 \|Associated morphology (attribute)\|	68245003 \|Spongy degeneration (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7008576029) - 733422008 -> 84676004 (246075003) View
246075003 \|Causative agent (attribute)\|	84676004 \|Prion (organism)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7008578028) - 733422008 -> 441862004 (370135005) View
370135005 \|Pathological process (attribute)\|	441862004 \|Infectious process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7115969020) - 733422008 -> 367601000119103 (116680003) View
116680003 \|Is a (attribute)\|	367601000119103 \|Hereditary amyloidosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
89449005 View
89449005	Systemic amyloidosis (disorder)	Systemic amyloidosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
106018006 View
106018006	Hereditary degenerative disease of central nervous system (disorder)	Hereditary degenerative disease of central nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
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
20484008 View
20484008	Prion disease (disorder)	Prion disease	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 (180d1b23-0df8-50e5-87e6-01f279bc8559) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E85.1	TRUE	ALWAYS E85.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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 (b0866a06-9d75-58c2-80e6-4ebbf55bec6a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G63.3	TRUE	ALWAYS G63.3 \| 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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