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Terminology chevron_right Concepts chevron_right 770626007

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Component

770626007

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital horner syndrome (disorder)

Shortest Term

Hội chứng horner bẩm sinh

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

Congenital horner syndrome (disorder)

SCTID: 770626007, Primitive, Active

770626007|Congenital horner syndrome (disorder)|

vi Hội chứng horner bẩm sinh
en Congenital claude bernard horner syndrome
en Congenital horner syndrome
en Congenital horner syndrome (disorder)

Expression

770626007 |Congenital horner syndrome (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
722997000 |Inherited autonomic nervous system disorder (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
1281810006 |Horner syndrome (disorder)| + 
66091009 |Congenital disease (disorder)| : 
        { 363698007 |Finding site (attribute)| = 90456006 |Sympathetic nerve structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
538661000003119 - hội chứng Horner bẩm sinh (vi) View
538661000003119	vi	Synonym (core metadata concept)	hội chứng Horner bẩm sinh	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3701689011 - Congenital Claude Bernard Horner syndrome (en) View
3701689011	en	Synonym (core metadata concept)	Congenital Claude Bernard Horner syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
3701688015 - Congenital Horner syndrome (en) View
3701688015	en	Synonym (core metadata concept)	Congenital Horner syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3701687013 - Congenital Horner syndrome (disorder) (en) View
3701687013	en	Fully specified name (core metadata concept)	Congenital Horner syndrome (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9638494027) - 770626007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9638495026) - 770626007 -> 271730003 (116680003) View
116680003 \|Is a (attribute)\|	271730003 \|Horner's syndrome pupil (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9638499021) - 770626007 -> 268163008 (116680003) View
116680003 \|Is a (attribute)\|	268163008 \|Congenital ptosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9638501029) - 770626007 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9638502020) - 770626007 -> 415219007 (363714003) View
363714003 \|Interprets (attribute)\|	415219007 \|Pupil constriction (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9638504021) - 770626007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9638506023) - 770626007 -> 38934000 (363698007) View
363698007 \|Finding site (attribute)\|	38934000 \|Upper eyelid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9648710020) - 770626007 -> 392406005 (363698007) View
363698007 \|Finding site (attribute)\|	392406005 \|Pupil structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9651242028) - 770626007 -> 53520000 (363698007) View
363698007 \|Finding site (attribute)\|	53520000 \|Autonomic nerve structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10515188028) - 770626007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10515189020) - 770626007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11168419023) - 770626007 -> 29696001 (116676008) View
116676008 \|Associated morphology (attribute)\|	29696001 \|Prolapse (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15533343020) - 770626007 -> 363953003 (363714003) View
363714003 \|Interprets (attribute)\|	363953003 \|Size of pupil (observable entity)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15648740021) - 770626007 -> 1281810006 (116680003) View
116680003 \|Is a (attribute)\|	1281810006 \|Horner syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15648742029) - 770626007 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15648743023) - 770626007 -> 90456006 (363698007) View
363698007 \|Finding site (attribute)\|	90456006 \|Sympathetic nerve structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13069850021) - 770626007 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9638497023) - 770626007 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9638498029) - 770626007 -> 722997000 (116680003) View
116680003 \|Is a (attribute)\|	722997000 \|Inherited autonomic nervous system disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9638503026) - 770626007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10515187022) - 770626007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1281810006 View
1281810006	Horner syndrome (disorder)	Horner syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
722997000 View
722997000	Inherited autonomic nervous system disorder (disorder)	Inherited autonomic nervous system disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	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

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 (9878cb50-64a4-54fb-ba0c-9c3af58362f1) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G90.2	TRUE	ALWAYS G90.2 \| 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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