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Terminology chevron_right Concepts chevron_right 1230020008

Production

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Component

1230020008

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital peripapillary staphyloma (disorder)

Shortest Term

Congenital peripapillary staphyloma

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 peripapillary staphyloma (disorder)

SCTID: 1230020008, Primitive, Active

1230020008|Congenital peripapillary staphyloma (disorder)|

en Congenital peripapillary staphyloma
en Congenital peripapillary staphyloma (disorder)

Expression

1230020008 |Congenital peripapillary staphyloma (disorder)|
 <<< 60505005 |Congenital anomaly of optic disc (disorder)| + 
24210004 |Congenital chorioretinal degeneration (disorder)| + 
95686007 |Chorioretinal atrophy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 81016008 |Optic disc structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 68703001 |Choroidal structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 5665001 |Retinal 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
5066434018 - Congenital peripapillary staphyloma (en) View
5066434018	en	Synonym (core metadata concept)	Congenital peripapillary staphyloma	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5066435017 - Congenital peripapillary staphyloma (disorder) (en) View
5066435017	en	Fully specified name (core metadata concept)	Congenital peripapillary staphyloma (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15221709022) - 1230020008 -> 60505005 (116680003) View
116680003 \|Is a (attribute)\|	60505005 \|Congenital anomaly of optic disc (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221710028) - 1230020008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221711029) - 1230020008 -> 81016008 (363698007) View
363698007 \|Finding site (attribute)\|	81016008 \|Optic disc structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221712020) - 1230020008 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221713026) - 1230020008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221714021) - 1230020008 -> 24210004 (116680003) View
116680003 \|Is a (attribute)\|	24210004 \|Congenital chorioretinal degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221715022) - 1230020008 -> 95686007 (116680003) View
116680003 \|Is a (attribute)\|	95686007 \|Chorioretinal atrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221716023) - 1230020008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221717025) - 1230020008 -> 68703001 (363698007) View
363698007 \|Finding site (attribute)\|	68703001 \|Choroidal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221718024) - 1230020008 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221719027) - 1230020008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221720022) - 1230020008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221721021) - 1230020008 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221722025) - 1230020008 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15221723024) - 1230020008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
95686007 View
95686007	Chorioretinal atrophy (disorder)	Chorioretinal atrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
24210004 View
24210004	Congenital chorioretinal degeneration (disorder)	Congenital chorioretinal degeneration	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
60505005 View
60505005	Congenital anomaly of optic disc (disorder)	Optic disc anomaly	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 (db41bf59-c53a-525e-b39a-7482166fef52) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q14.2	TRUE	ALWAYS Q14.2 \| 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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