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Terminology chevron_right Concepts chevron_right 711482008

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Component

711482008

The component that hold information about this concept.

Fully Specified Name (FSN)

Cerebroretinal microangiopathy with calcifications and cysts (disorder)

Shortest Term

Coats plus 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

Cerebroretinal microangiopathy with calcifications and cysts (disorder)

SCTID: 711482008, Primitive, Active

711482008|Cerebroretinal microangiopathy with calcifications and cysts (disorder)|

en Cerebroretinal microangiopathy with calcifications and cysts
en Cerebroretinal microangiopathy with calcifications and cysts (disorder)
en Coats plus syndrome

Expression

711482008 |Cerebroretinal microangiopathy with calcifications and cysts (disorder)|
 <<< 422840005 |Mass lesion of brain (finding)| + 
29555009 |Retinal disorder (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| + 
17944005 |Cerebral calcification (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
106018006 |Hereditary degenerative disease of central nervous system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 18115005 |Pathologic calcification, calcified structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 83678007 |Cerebral structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 4147007 |Mass (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3078853010 - Cerebroretinal microangiopathy with calcifications and cysts (en) View
3078853010	en	Synonym (core metadata concept)	Cerebroretinal microangiopathy with calcifications and cysts	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3078911010 - Cerebroretinal microangiopathy with calcifications and cysts (disorder) (en) View
3078911010	en	Fully specified name (core metadata concept)	Cerebroretinal microangiopathy with calcifications and cysts (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3078849013 - Coats plus syndrome (en) View
3078849013	en	Synonym (core metadata concept)	Coats plus syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6232349020) - 711482008 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12088308029) - 711482008 -> 106018006 (116680003) View
116680003 \|Is a (attribute)\|	106018006 \|Hereditary degenerative disease of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6232351024) - 711482008 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6232353022) - 711482008 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6246984026) - 711482008 -> 18115005 (116676008) View
116676008 \|Associated morphology (attribute)\|	18115005 \|Pathologic calcification, calcified structure (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6874014024) - 711482008 -> 18115005 (116676008) View
116676008 \|Associated morphology (attribute)\|	18115005 \|Pathologic calcification, calcified structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6874015020) - 711482008 -> 83678007 (363698007) View
363698007 \|Finding site (attribute)\|	83678007 \|Cerebral structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6232345025) - 711482008 -> 422840005 (116680003) View
116680003 \|Is a (attribute)\|	422840005 \|Mass lesion of brain (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6232346029) - 711482008 -> 29555009 (116680003) View
116680003 \|Is a (attribute)\|	29555009 \|Retinal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6232347022) - 711482008 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6232348028) - 711482008 -> 17944005 (116680003) View
116680003 \|Is a (attribute)\|	17944005 \|Cerebral calcification (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6232350020) - 711482008 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6232355026) - 711482008 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6246985025) - 711482008 -> 4147007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4147007 \|Mass (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
106018006 View
106018006	Hereditary degenerative disease of central nervous system (disorder)	Hereditary degenerative disease of central nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
17944005 View
17944005	Cerebral calcification (disorder)	Cerebral calcification	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
422840005 View
422840005	Mass lesion of brain (finding)	Brain mass	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
29555009 View
29555009	Retinal disorder (disorder)	Retinopathy	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 (dfdca060-eb7a-5f7d-b379-69107cdfb9fa) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.0	TRUE	ALWAYS H35.0	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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