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Terminology chevron_right Concepts chevron_right 716166002

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Component

716166002

The component that hold information about this concept.

Fully Specified Name (FSN)

Microcornea with glaucoma and absent frontal sinus syndrome (disorder)

Shortest Term

Microcornea with glaucoma and absent frontal sinus 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 with glaucoma and absent frontal sinus syndrome (disorder)

SCTID: 716166002, Primitive, Active

716166002|Microcornea with glaucoma and absent frontal sinus syndrome (disorder)|

vi Giác mạc nhỏ kèm hội chứng tăng nhãn áp và không có xoang trán
en Microcornea with glaucoma and absent frontal sinus syndrome
en Microcornea with glaucoma and absent frontal sinus syndrome (disorder)

Expression

716166002 |Microcornea with glaucoma and absent frontal sinus syndrome (disorder)|
 <<< 363070008 |Developmental hereditary disorder (disorder)| + 
26098002 |Microcornea (disorder)| + 
105973004 |Disorder of frontal sinus (disorder)| + 
128275006 |Congenital anomaly of nasal sinuses (disorder)| + 
204113001 |Congenital glaucoma (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1303834006 |Abnormal smallness (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 28726007 |Corneal structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 418560003 |Absence (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 55060009 |Frontal sinus 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
439331000003118 - giác mạc nhỏ kèm hội chứng tăng nhãn áp và không có xoang trán (vi) View
439331000003118	vi	Synonym (core metadata concept)	giác mạc nhỏ kèm hội chứng tăng nhãn áp và không có xoang trán	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3304945016 - Microcornea with glaucoma and absent frontal sinus syndrome (en) View
3304945016	en	Synonym (core metadata concept)	Microcornea with glaucoma and absent frontal sinus syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3304944017 - Microcornea with glaucoma and absent frontal sinus syndrome (disorder) (en) View
3304944017	en	Fully specified name (core metadata concept)	Microcornea with glaucoma and absent frontal sinus syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10545348022) - 716166002 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15898923020) - 716166002 -> 1303834006 (116676008) View
116676008 \|Associated morphology (attribute)\|	1303834006 \|Abnormal smallness (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6575594020) - 716166002 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13069627029) - 716166002 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13185250026) - 716166002 -> 418560003 (116676008) View
116676008 \|Associated morphology (attribute)\|	418560003 \|Absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6574919025) - 716166002 -> 702626005 (116680003) View
116680003 \|Is a (attribute)\|	702626005 \|Congenital absence (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6574920020) - 716166002 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6574922028) - 716166002 -> 28726007 (363698007) View
363698007 \|Finding site (attribute)\|	28726007 \|Corneal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6574923022) - 716166002 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6574924027) - 716166002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6574925026) - 716166002 -> 55060009 (363698007) View
363698007 \|Finding site (attribute)\|	55060009 \|Frontal sinus structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6575595021) - 716166002 -> 55060009 (363698007) View
363698007 \|Finding site (attribute)\|	55060009 \|Frontal sinus structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10516109027) - 716166002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10516110021) - 716166002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10516113023) - 716166002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10545347028) - 716166002 -> 28726007 (363698007) View
363698007 \|Finding site (attribute)\|	28726007 \|Corneal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6574913029) - 716166002 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6574914024) - 716166002 -> 26098002 (116680003) View
116680003 \|Is a (attribute)\|	26098002 \|Microcornea (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6574915020) - 716166002 -> 105973004 (116680003) View
116680003 \|Is a (attribute)\|	105973004 \|Disorder of frontal sinus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6574916021) - 716166002 -> 128275006 (116680003) View
116680003 \|Is a (attribute)\|	128275006 \|Congenital anomaly of nasal sinuses (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6574917028) - 716166002 -> 204113001 (116680003) View
116680003 \|Is a (attribute)\|	204113001 \|Congenital glaucoma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6574918022) - 716166002 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6574921024) - 716166002 -> 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
204113001 View
204113001	Congenital glaucoma (disorder)	Congenital glaucoma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
26098002 View
26098002	Microcornea (disorder)	Microcornea	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
105973004 View
105973004	Disorder of frontal sinus (disorder)	Bệnh xoang trán	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
128275006 View
128275006	Congenital anomaly of nasal sinuses (disorder)	Congenital anomaly of nasal sinuses	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 (47d4f0d4-ae79-5f3e-ae66-ecd603e77501) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q34.8	TRUE	ALWAYS Q34.8	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 (cce0d858-b572-5b8c-a112-72ec5a6b27b9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q15.0	TRUE	ALWAYS Q15.0	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)\|
ExtendedMap object (ee006ced-1abf-5fd9-a99b-6de2f28e4363) 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 (fd3f4dfd-f2b6-5259-8fdb-df50c6820606) 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)\|

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