dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 722437006

Production

add

Component

722437006

The component that hold information about this concept.

Fully Specified Name (FSN)

Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder)

Shortest Term

Ectopia lentis, chorioretinal dystrophy, myopia syndrome

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

Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder)

SCTID: 722437006, Primitive, Active

722437006|Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder)|

en Ectopia lentis, chorioretinal dystrophy, myopia syndrome
en Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder)

Expression

722437006 |Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder)|
 <<< 74969002 |Congenital ectopic lens (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| + 
24210004 |Congenital chorioretinal degeneration (disorder)| + 
314407005 |Retinal dystrophy (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (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)| }
        { 116676008 |Associated morphology (attribute)| = 416286003 |Congenital ectopia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 78076003 |Structure of lens of eye (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (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)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3332071017 - Ectopia lentis, chorioretinal dystrophy, myopia syndrome (en) View
3332071017	en	Synonym (core metadata concept)	Ectopia lentis, chorioretinal dystrophy, myopia syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3332070016 - Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder) (en) View
3332070016	en	Fully specified name (core metadata concept)	Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6791529022) - 722437006 -> 62585004 (116680003) View
116680003 \|Is a (attribute)\|	62585004 \|Degenerative disorder of eye (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6791532020) - 722437006 -> 302893000 (116680003) View
116680003 \|Is a (attribute)\|	302893000 \|Chorioretinal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6791538024) - 722437006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514971026) - 722437006 -> 128534003 (116680003) View
116680003 \|Is a (attribute)\|	128534003 \|Congenital anomaly of posterior segment of eye (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10545239026) - 722437006 -> 303295006 (363698007) View
363698007 \|Finding site (attribute)\|	303295006 \|Choroidal and/or retinal structures (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13648729026) - 722437006 -> 314407005 (116680003) View
116680003 \|Is a (attribute)\|	314407005 \|Retinal dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13648730020) - 722437006 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13648754026) - 722437006 -> 24210004 (116680003) View
116680003 \|Is a (attribute)\|	24210004 \|Congenital chorioretinal degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13648755025) - 722437006 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13648756029) - 722437006 -> 68703001 (363698007) View
363698007 \|Finding site (attribute)\|	68703001 \|Choroidal structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13648757022) - 722437006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13069395022) - 722437006 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791534021) - 722437006 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6791536023) - 722437006 -> 303295006 (363698007) View
363698007 \|Finding site (attribute)\|	303295006 \|Choroidal and/or retinal structures (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6791537025) - 722437006 -> 416286003 (116676008) View
116676008 \|Associated morphology (attribute)\|	416286003 \|Congenital ectopia (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6791539027) - 722437006 -> 78076003 (363698007) View
363698007 \|Finding site (attribute)\|	78076003 \|Structure of lens of eye (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6795067021) - 722437006 -> 416286003 (116676008) View
116676008 \|Associated morphology (attribute)\|	416286003 \|Congenital ectopia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6795068027) - 722437006 -> 78076003 (363698007) View
363698007 \|Finding site (attribute)\|	78076003 \|Structure of lens of eye (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514969026) - 722437006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514972022) - 722437006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514973028) - 722437006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10545240029) - 722437006 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791530028) - 722437006 -> 74969002 (116680003) View
116680003 \|Is a (attribute)\|	74969002 \|Congenital ectopic lens (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791531029) - 722437006 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791533026) - 722437006 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791535022) - 722437006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	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
24210004 View
24210004	Congenital chorioretinal degeneration (disorder)	Congenital chorioretinal degeneration	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
314407005 View
314407005	Retinal dystrophy (disorder)	Retinal dystrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
74969002 View
74969002	Congenital ectopic lens (disorder)	Ectopia lentis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	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 (3f1e172a-02a7-5297-a79e-2e399a3c2d1e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q15.8	TRUE	ALWAYS Q15.8 \| 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)\|

Terminology chevron_right Concepts chevron_right 722437006

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches