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Terminology chevron_right Concepts chevron_right 196286005

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Component

196286005

The component that hold information about this concept.

Fully Specified Name (FSN)

Dentinogenesis imperfecta (disorder)

Shortest Term

Dentinogenesis imperfecta

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

Dentinogenesis imperfecta (disorder)

SCTID: 196286005, Primitive, Active

196286005|Dentinogenesis imperfecta (disorder)|

en Hereditary opalescent dentin
en Dentinogenesis imperfecta
en Dentinogenesis imperfecta (disorder)

Expression

196286005 |Dentinogenesis imperfecta (disorder)|
 <<< 363070008 |Developmental hereditary disorder (disorder)| + 
1148766007 |Hereditary disorder of tooth (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
46557008 |Disorder of hard tissues of teeth (disorder)| + 
422977003 |Congenital anomaly of tooth (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 84540008 |Dentin 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
4551866016 - Hereditary opalescent dentin (en) View
4551866016	en	Synonym (core metadata concept)	Hereditary opalescent dentin	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
301910015 - Dentinogenesis imperfecta (en) View
301910015	en	Synonym (core metadata concept)	Dentinogenesis imperfecta	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
580498015 - Dentinogenesis imperfecta (disorder) (en) View
580498015	en	Fully specified name (core metadata concept)	Dentinogenesis imperfecta (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (20678028) - 196286005 -> 234960009 (116680003) View
116680003 \|Is a (attribute)\|	234960009 \|Hereditary or idiopathic disturbance of tooth structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (464204029) - 196286005 -> 38199008 (363698007) View
363698007 \|Finding site (attribute)\|	38199008 \|Tooth structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2990741029) - 196286005 -> 422977003 (116680003) View
116680003 \|Is a (attribute)\|	422977003 \|Congenital anomaly of tooth (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6106035024) - 196286005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10526999023) - 196286005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10527000021) - 196286005 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13717770022) - 196286005 -> 1148766007 (116680003) View
116680003 \|Is a (attribute)\|	1148766007 \|Hereditary disorder of tooth (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13717820028) - 196286005 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13717829027) - 196286005 -> 46557008 (116680003) View
116680003 \|Is a (attribute)\|	46557008 \|Disorder of hard tissues of teeth (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13717830021) - 196286005 -> 84540008 (363698007) View
363698007 \|Finding site (attribute)\|	84540008 \|Dentin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13724294025) - 196286005 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4988084026) - 196286005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4988085025) - 196286005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5019903023) - 196286005 -> 38199008 (363698007) View
363698007 \|Finding site (attribute)\|	38199008 \|Tooth structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3358558023) - 196286005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3358559026) - 196286005 -> 38199008 (363698007) View
363698007 \|Finding site (attribute)\|	38199008 \|Tooth structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (464201021) - 196286005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (464206027) - 196286005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (20677022) - 196286005 -> 79723009 (116680003) View
116680003 \|Is a (attribute)\|	79723009 \|Congenital anomaly of teeth (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (464202025) - 196286005 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (464207020) - 196286005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1720888028) - 196286005 -> 74262004 (363698007) View
363698007 \|Finding site (attribute)\|	74262004 \|Oral cavity structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1936988026) - 196286005 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2251893026) - 196286005 -> 119253004 (363698007) View
363698007 \|Finding site (attribute)\|	119253004 \|Upper aerodigestive tract structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1720889020) - 196286005 -> 89545001 (363698007) View
363698007 \|Finding site (attribute)\|	89545001 \|Face structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (464203024) - 196286005 -> 21974007 (363698007) View
363698007 \|Finding site (attribute)\|	21974007 \|Tongue structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (464205028) - 196286005 -> 661005 (363698007) View
363698007 \|Finding site (attribute)\|	661005 \|Jaw region structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (464208026) - 196286005 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1148766007 View
1148766007	Hereditary disorder of tooth (disorder)	Hereditary disorder of tooth	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
422977003 View
422977003	Congenital anomaly of tooth (disorder)	Congenital anomaly of tooth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
46557008 View
46557008	Disorder of hard tissues of teeth (disorder)	Teeth hard tissue diseases	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

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
67504007 View
67504007	Shell teeth (disorder)	Ghost teeth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
733468006 View
733468006	Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome (disorder)	Suarez stickler syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
717823001 View
717823001	Chondrodysplasia, dentinogenesis imperfecta, joint laxity syndrome (disorder)	Goldblatt syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
721089006 View
721089006	Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (disorder)	Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
63890001 View
63890001	Osteogenesis imperfecta with blue sclerae and dentinogenesis imperfecta (disorder)	Osteogenesis imperfecta type ib	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234968002 View
234968002	Dentinogenesis imperfecta - shield's type i (disorder)	Dentinogenesis imperfecta - shield's type i	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234969005 View
234969005	Dentinogenesis imperfecta - shield's type ii (disorder)	Capdepont teeth	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234970006 View
234970006	Dentinogenesis imperfecta - shield's type iii (disorder)	Brandywine type of dentinogenesis imperfecta	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
279309008 View
279309008	Osteogenesis imperfecta, type iv b (disorder)	Osteogenesis imperfecta, type iv b	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (e0645f2a-e5ec-58ed-82ee-95019c8c8fbf) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K00.5	TRUE	ALWAYS K00.5	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)\|

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