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Terminology chevron_right Concepts chevron_right 45484000

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Component

45484000

The component that hold information about this concept.

Fully Specified Name (FSN)

Partial ablepharon (disorder)

Shortest Term

Partial ablepharon

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

Partial ablepharon (disorder)

SCTID: 45484000, Defined, Active

45484000|Partial ablepharon (disorder)|

en Partial ablepharon
en Partial ablepharon (disorder)

Expression

45484000 |Partial ablepharon (disorder)|
 === 13401001 |Ablepharon (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 418560003 |Absence (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 709293002 |Eyelid part (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
75830018 - Partial ablepharon (en) View
75830018	en	Synonym (core metadata concept)	Partial ablepharon	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
782728019 - Partial ablepharon (disorder) (en) View
782728019	en	Fully specified name (core metadata concept)	Partial ablepharon (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6035483022) - 45484000 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13185276026) - 45484000 -> 418560003 (116676008) View
116676008 \|Associated morphology (attribute)\|	418560003 \|Absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10516853024) - 45484000 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3325140021) - 45484000 -> 88456007 (116676008) View
116676008 \|Associated morphology (attribute)\|	88456007 \|Congenital partial absence (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3325141020) - 45484000 -> 80243003 (363698007) View
363698007 \|Finding site (attribute)\|	80243003 \|Eyelid structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4983299023) - 45484000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5967699028) - 45484000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6035484027) - 45484000 -> 709293002 (363698007) View
363698007 \|Finding site (attribute)\|	709293002 \|Eyelid part (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4992482028) - 45484000 -> 80243003 (363698007) View
363698007 \|Finding site (attribute)\|	80243003 \|Eyelid structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5017743025) - 45484000 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (785535028) - 45484000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (518405026) - 45484000 -> 80243003 (363698007) View
363698007 \|Finding site (attribute)\|	80243003 \|Eyelid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (785536027) - 45484000 -> 88456007 (116676008) View
116676008 \|Associated morphology (attribute)\|	88456007 \|Congenital partial absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1767833026) - 45484000 -> 363654007 (363698007) View
363698007 \|Finding site (attribute)\|	363654007 \|Structure of orbit proper (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2030877020) - 45484000 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (222079028) - 45484000 -> 13401001 (116680003) View
116680003 \|Is a (attribute)\|	13401001 \|Ablepharon (disorder)\|	0	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
724016008 View
724016008	Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome (disorder)	Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
63935007 View
63935007	Congenital absence of eyelash (disorder)	Agenesis of cilia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
204208005 View
204208005	Agenesis of punctum lacrimale (disorder)	Agenesis of lacrimal punctum	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (085a5632-f0ac-59a8-9977-706a4fdafe0b) 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)\|

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