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Terminology chevron_right Concepts chevron_right 715980003

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Component

715980003

The component that hold information about this concept.

Fully Specified Name (FSN)

Encephalopathy due to sulfite oxidase deficiency (disorder)

Shortest Term

Encephalopathy due to sulfite oxidase deficiency

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

Encephalopathy due to sulfite oxidase deficiency (disorder)

SCTID: 715980003, Defined, Active

715980003|Encephalopathy due to sulfite oxidase deficiency (disorder)|

en Encephalopathy due to sulfite oxidase deficiency
en Encephalopathy due to sulfite oxidase deficiency (disorder)
en Encephalopathy due to sulphite oxidase deficiency

Expression

715980003 |Encephalopathy due to sulfite oxidase deficiency (disorder)|
 === 20842008 |Luxation of eye (disorder)| + 
10810001 |Disorder of lens (disorder)| + 
81308009 |Disorder of brain (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| + 
87536007 |Central nervous system complication (disorder)| : 
        { 42752001 |Due to (attribute)| = 367368009 |Sulfite oxidase deficiency (disorder)| }
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 87642003 |Dislocation (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 78076003 |Structure of lens of eye (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3303629014 - Encephalopathy due to sulfite oxidase deficiency (en) View
3303629014	en	Synonym (core metadata concept)	Encephalopathy due to sulfite oxidase deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3303628018 - Encephalopathy due to sulfite oxidase deficiency (disorder) (en) View
3303628018	en	Fully specified name (core metadata concept)	Encephalopathy due to sulfite oxidase deficiency (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3304304018 - Encephalopathy due to sulphite oxidase deficiency (en) View
3304304018	en	Synonym (core metadata concept)	Encephalopathy due to sulphite oxidase deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10539390021) - 715980003 -> 11131000119108 (116680003) View
116680003 \|Is a (attribute)\|	11131000119108 \|Anomaly of eye (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15281055024) - 715980003 -> 20842008 (116680003) View
116680003 \|Is a (attribute)\|	20842008 \|Luxation of eye (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13951605027) - 715980003 -> 87536007 (116680003) View
116680003 \|Is a (attribute)\|	87536007 \|Central nervous system complication (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594655028) - 715980003 -> 367368009 (42752001) View
42752001 \|Due to (attribute)\|	367368009 \|Sulfite oxidase deficiency (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594661025) - 715980003 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594656027) - 715980003 -> 10810001 (116680003) View
116680003 \|Is a (attribute)\|	10810001 \|Disorder of lens (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594657020) - 715980003 -> 81308009 (116680003) View
116680003 \|Is a (attribute)\|	81308009 \|Disorder of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594658026) - 715980003 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594659023) - 715980003 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594660029) - 715980003 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594662021) - 715980003 -> 87642003 (116676008) View
116676008 \|Associated morphology (attribute)\|	87642003 \|Dislocation (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594663027) - 715980003 -> 78076003 (363698007) View
363698007 \|Finding site (attribute)\|	78076003 \|Structure of lens of eye (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
87536007 View
87536007	Central nervous system complication (disorder)	Central nervous system complication	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
20842008 View
20842008	Luxation of eye (disorder)	Luxation of eye	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
10810001 View
10810001	Disorder of lens (disorder)	Disorder of lens	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
81308009 View
81308009	Disorder of brain (disorder)	Encephalopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept 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
363343008 View
363343008	Hereditary disorder of the visual system (disorder)	Hereditary disorder of the visual 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 (02fa9996-5be4-5172-983c-09991e9b602a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E72.1	TRUE	ALWAYS E72.1 \| 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)\|

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