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Terminology chevron_right Concepts chevron_right 774151000

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Component

774151000

The component that hold information about this concept.

Fully Specified Name (FSN)

Ferro-cerebro-cutaneous syndrome (disorder)

Shortest Term

Hội chứng da - não - não

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

Ferro-cerebro-cutaneous syndrome (disorder)

SCTID: 774151000, Primitive, Active

774151000|Ferro-cerebro-cutaneous syndrome (disorder)|

vi Hội chứng da - não - não
en Cerebro-cutaneous syndrome with iron overload
en Ferro-cerebro-cutaneous syndrome
en Ferro-cerebro-cutaneous syndrome (disorder)

Expression

774151000 |Ferro-cerebro-cutaneous syndrome (disorder)|
 <<< 363080007 |Digestive system hereditary disorder (disorder)| + 
235903001 |Metabolic and genetic disorder affecting the liver (disorder)| + 
106018006 |Hereditary degenerative disease of central nervous system (disorder)| + 
1162976004 |X-linked recessive hereditary disease (disorder)| + 
52522001 |Degenerative brain disorder (disorder)| + 
60737008 |Iron overload (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
        { 246075003 |Causative agent (attribute)| = 767270007 |Iron and iron compound (substance)| }
        { 363698007 |Finding site (attribute)| = 10200004 |Liver structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
453401000003115 - hội chứng da - não - não (vi) View
453401000003115	vi	Synonym (core metadata concept)	hội chứng da - não - não	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3728150018 - Cerebro-cutaneous syndrome with iron overload (en) View
3728150018	en	Synonym (core metadata concept)	Cerebro-cutaneous syndrome with iron overload	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3728151019 - Ferro-cerebro-cutaneous syndrome (en) View
3728151019	en	Synonym (core metadata concept)	Ferro-cerebro-cutaneous syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3728152014 - Ferro-cerebro-cutaneous syndrome (disorder) (en) View
3728152014	en	Fully specified name (core metadata concept)	Ferro-cerebro-cutaneous syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10624901025) - 774151000 -> 81308009 (116680003) View
116680003 \|Is a (attribute)\|	81308009 \|Disorder of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15805433021) - 774151000 -> 52522001 (116680003) View
116680003 \|Is a (attribute)\|	52522001 \|Degenerative brain disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624908020) - 774151000 -> 128430005 (116680003) View
116680003 \|Is a (attribute)\|	128430005 \|X-linked hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14011008027) - 774151000 -> 1162976004 (116680003) View
116680003 \|Is a (attribute)\|	1162976004 \|X-linked recessive hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624903027) - 774151000 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10624904022) - 774151000 -> 80690008 (116680003) View
116680003 \|Is a (attribute)\|	80690008 \|Degenerative disease of the central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10624905023) - 774151000 -> 33359002 (116676008) View
116676008 \|Associated morphology (attribute)\|	33359002 \|Degeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12095784029) - 774151000 -> 107669003 (116676008) View
116676008 \|Associated morphology (attribute)\|	107669003 \|Degenerative abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12095785028) - 774151000 -> 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 (10624900029) - 774151000 -> 767270007 (246075003) View
246075003 \|Causative agent (attribute)\|	767270007 \|Iron and iron compound (substance)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624909028) - 774151000 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624899023) - 774151000 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624902021) - 774151000 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624906024) - 774151000 -> 60737008 (116680003) View
116680003 \|Is a (attribute)\|	60737008 \|Iron overload (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624907026) - 774151000 -> 235903001 (116680003) View
116680003 \|Is a (attribute)\|	235903001 \|Metabolic and genetic disorder affecting the liver (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1162976004 View
1162976004	X-linked recessive hereditary disease (disorder)	X-linked recessive hereditary disease	900000000000074008 \|Necessary but not sufficient concept 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
52522001 View
52522001	Degenerative brain disorder (disorder)	Cerebral degeneration	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
60737008 View
60737008	Iron overload (disorder)	Iron excess	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
235903001 View
235903001	Metabolic and genetic disorder affecting the liver (disorder)	Rối loạn chuyển hóa và di truyền ảnh hưởng đến gan	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	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 (9922c896-8d95-5671-9a8b-27af5a7c8f85) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G23.0	TRUE	ALWAYS G23.0 \| 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)\|

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