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Terminology chevron_right Concepts chevron_right 771342004

Production

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Component

771342004

The component that hold information about this concept.

Fully Specified Name (FSN)

Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder)

Shortest Term

Mrcs 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

Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder)

SCTID: 771342004, Primitive, Active

771342004|Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder)|

en Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome
en Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder)
en Mrcs (microcornea, rod-cone dystrophy, cataract, posterior staphyloma) syndrome
en Mrcs syndrome

Expression

771342004 |Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder)|
 <<< 41799005 |Hereditary retinal dystrophy (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
193570009 |Cataract (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 128305008 |Abnormally opaque structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 78076003 |Structure of lens of eye (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3705835018 - Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (en) View
3705835018	en	Synonym (core metadata concept)	Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3705834019 - Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder) (en) View
3705834019	en	Fully specified name (core metadata concept)	Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3705837014 - MRCS (microcornea, rod-cone dystrophy, cataract, posterior staphyloma) syndrome (en) View
3705837014	en	Synonym (core metadata concept)	MRCS (microcornea, rod-cone dystrophy, cataract, posterior staphyloma) syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3705836017 - MRCS syndrome (en) View
3705836017	en	Synonym (core metadata concept)	MRCS syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9662744028) - 771342004 -> 128306009 (116676008) View
116676008 \|Associated morphology (attribute)\|	128306009 \|Cataract (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11344416025) - 771342004 -> 128305008 (116676008) View
116676008 \|Associated morphology (attribute)\|	128305008 \|Abnormally opaque structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9662745027) - 771342004 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9662746026) - 771342004 -> 78076003 (363698007) View
363698007 \|Finding site (attribute)\|	78076003 \|Structure of lens of eye (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9662747024) - 771342004 -> 193570009 (116680003) View
116680003 \|Is a (attribute)\|	193570009 \|Cataract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9662748025) - 771342004 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9662749022) - 771342004 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9662750022) - 771342004 -> 41799005 (116680003) View
116680003 \|Is a (attribute)\|	41799005 \|Hereditary retinal dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
193570009 View
193570009	Cataract (disorder)	Cataract	900000000000073002 \|Sufficiently defined by necessary conditions 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
41799005 View
41799005	Hereditary retinal dystrophy (disorder)	Hereditary retinal dystrophy	900000000000074008 \|Necessary but not sufficient concept 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 (3a792ee7-96a9-565a-a1f0-78d8ebde8833) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.5	TRUE	ALWAYS H35.5 \| 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)\|
ExtendedMap object (86ea76b4-c914-5942-912d-2c60bf74996f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.5	TRUE	ALWAYS H35.5	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)\|
ExtendedMap object (d517e7de-d7d0-536f-8d74-5b1c3c0f3dfd) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H15.8	TRUE	ALWAYS H15.8	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)\|
ExtendedMap object (d5942a00-565c-5a97-9172-ac755ecb7958) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q13.4	TRUE	ALWAYS Q13.4	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)\|
ExtendedMap object (e7bde132-dcc7-5d08-bca3-a9e6891abf21) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q13.4	TRUE	ALWAYS Q13.4 \| MAPPED FOLLOWING WHO GUIDANCE	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)\|
ExtendedMap object (eebd4a76-7641-54f7-b10b-98dc57661aa4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H26.9	TRUE	ALWAYS H26.9	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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