dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 708541009

Production

add

Component

708541009

The component that hold information about this concept.

Fully Specified Name (FSN)

Complete ablepharon (disorder)

Shortest Term

Agenesis of eyelid

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

Complete ablepharon (disorder)

SCTID: 708541009, Defined, Active

708541009|Complete ablepharon (disorder)|

en Agenesis of eyelid
en Complete ablepharon
en Complete ablepharon (disorder)
en Congenital absence of eyelid

Expression

708541009 |Complete ablepharon (disorder)|
 === 13401001 |Ablepharon (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 782173000 |Agenesis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 265782007 |Entire eyelid (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
3034852016 - Agenesis of eyelid (en) View
3034852016	en	Synonym (core metadata concept)	Agenesis of eyelid	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3034841010 - Complete ablepharon (en) View
3034841010	en	Synonym (core metadata concept)	Complete ablepharon	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3034859013 - Complete ablepharon (disorder) (en) View
3034859013	en	Fully specified name (core metadata concept)	Complete ablepharon (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3034825014 - Congenital absence of eyelid (en) View
3034825014	en	Synonym (core metadata concept)	Congenital absence of eyelid	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5980707024) - 708541009 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10520673020) - 708541009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11183977025) - 708541009 -> 782173000 (116676008) View
116676008 \|Associated morphology (attribute)\|	782173000 \|Agenesis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5980706026) - 708541009 -> 13401001 (116680003) View
116680003 \|Is a (attribute)\|	13401001 \|Ablepharon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5980708025) - 708541009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5980709022) - 708541009 -> 265782007 (363698007) View
363698007 \|Finding site (attribute)\|	265782007 \|Entire eyelid (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
13401001 View
13401001	Ablepharon (disorder)	Open eye	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 (3f126d00-aebe-52e0-a14d-4bad67c906f3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q10.3	TRUE	ALWAYS Q10.3	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)\|

Terminology chevron_right Concepts chevron_right 708541009

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches