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Terminology chevron_right Concepts chevron_right 718691008

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Component

718691008

The component that hold information about this concept.

Fully Specified Name (FSN)

Isolated cryptophthalmos (disorder)

Shortest Term

Isolated cryptophthalmia

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

Isolated cryptophthalmos (disorder)

SCTID: 718691008, Primitive, Active

718691008|Isolated cryptophthalmos (disorder)|

en Isolated cryptophthalmia
en Isolated cryptophthalmos
en Isolated cryptophthalmos (disorder)

Expression

718691008 |Isolated cryptophthalmos (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| + 
400951005 |Cryptophthalmos (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 80243003 |Eyelid 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
3313233017 - Isolated cryptophthalmia (en) View
3313233017	en	Synonym (core metadata concept)	Isolated cryptophthalmia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3313232010 - Isolated cryptophthalmos (en) View
3313232010	en	Synonym (core metadata concept)	Isolated cryptophthalmos	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3313231015 - Isolated cryptophthalmos (disorder) (en) View
3313231015	en	Fully specified name (core metadata concept)	Isolated cryptophthalmos (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13069086021) - 718691008 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6612864027) - 718691008 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10522996025) - 718691008 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10522997023) - 718691008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6612861024) - 718691008 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6612862028) - 718691008 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6612863022) - 718691008 -> 400951005 (116680003) View
116680003 \|Is a (attribute)\|	400951005 \|Cryptophthalmos (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6612865026) - 718691008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6612866025) - 718691008 -> 80243003 (363698007) View
363698007 \|Finding site (attribute)\|	80243003 \|Eyelid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
400951005 View
400951005	Cryptophthalmos (disorder)	Cryptophthalmia	900000000000074008 \|Necessary but not sufficient concept 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
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 (2a9a98b0-1bcf-5ba7-b41a-8eef2504c60c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q11.2	TRUE	ALWAYS Q11.2 \| 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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