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Terminology chevron_right Concepts chevron_right 405809000

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Component

405809000

The component that hold information about this concept.

Fully Specified Name (FSN)

Ocular motor apraxia cogan type (disorder)

Shortest Term

Ocular motor apraxia cogan type

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

Ocular motor apraxia cogan type (disorder)

SCTID: 405809000, Primitive, Active

405809000|Ocular motor apraxia cogan type (disorder)|

en Congenital saccade initiation failure
en Ocular motor apraxia cogan type
en Ocular motor apraxia cogan type (disorder)
en Oculomotor apraxia - cogan type

Expression

405809000 |Ocular motor apraxia cogan type (disorder)|
 <<< 127329003 |Congenital anomaly of visual system (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
193662007 |Oculomotor apraxia (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 49549006 |Structure of visual system (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
5045006017 - Congenital saccade initiation failure (en) View
5045006017	en	Synonym (core metadata concept)	Congenital saccade initiation failure	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
5045005018 - Ocular motor apraxia Cogan type (en) View
5045005018	en	Synonym (core metadata concept)	Ocular motor apraxia Cogan type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
5045004019 - Ocular motor apraxia Cogan type (disorder) (en) View
5045004019	en	Fully specified name (core metadata concept)	Ocular motor apraxia Cogan type (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2149639013 - Oculomotor apraxia - Cogan type (disorder) (en) View
2149639013	en	Fully specified name (core metadata concept)	Oculomotor apraxia - Cogan type (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
2157583012 - Oculomotor apraxia - Cogan type (en) View
2157583012	en	Synonym (core metadata concept)	Oculomotor apraxia - Cogan type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15164819024) - 405809000 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15164821025) - 405809000 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15164822021) - 405809000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15164823027) - 405809000 -> 127329003 (116680003) View
116680003 \|Is a (attribute)\|	127329003 \|Congenital anomaly of visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15164824022) - 405809000 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15164825023) - 405809000 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15164826024) - 405809000 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2746170024) - 405809000 -> 49549006 (363698007) View
363698007 \|Finding site (attribute)\|	49549006 \|Structure of visual system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2746171023) - 405809000 -> 31763002 (363714003) View
363714003 \|Interprets (attribute)\|	31763002 \|Ocular motility observable (observable entity)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3326441022) - 405809000 -> 313088003 (363714003) View
363714003 \|Interprets (attribute)\|	313088003 \|Ocular muscle balance (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3326442026) - 405809000 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2746169023) - 405809000 -> 313088003 (363714003) View
363714003 \|Interprets (attribute)\|	313088003 \|Ocular muscle balance (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2746172027) - 405809000 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2495908025) - 405809000 -> 371398005 (363698007) View
363698007 \|Finding site (attribute)\|	371398005 \|Eye region structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2621582027) - 405809000 -> 399898009 (116676008) View
116676008 \|Associated morphology (attribute)\|	399898009 \|Misalignment (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2467376025) - 405809000 -> 193662007 (116680003) View
116680003 \|Is a (attribute)\|	193662007 \|Oculomotor apraxia (disorder)\|	0	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
193662007 View
193662007	Oculomotor apraxia (disorder)	Oculomotor apraxia	900000000000074008 \|Necessary but not sufficient concept 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
127329003 View
127329003	Congenital anomaly of visual system (disorder)	Congenital anomaly of visual system	900000000000073002 \|Sufficiently defined by necessary conditions 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 (68825126-8716-553b-8a46-92ee2e7790d4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H51.8	TRUE	ALWAYS H51.8	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)\|

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