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Terminology chevron_right Concepts chevron_right 234969005

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Component

234969005

The component that hold information about this concept.

Fully Specified Name (FSN)

Dentinogenesis imperfecta - shield's type ii (disorder)

Shortest Term

Capdepont teeth

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 - shield's type ii (disorder)

SCTID: 234969005, Primitive, Active

234969005|Dentinogenesis imperfecta - shield's type ii (disorder)|

en Capdepont teeth
en Dentinogenesis imperfecta without osteogenesis imperfecta
en Hereditary opalescent dentine
en Dentinogenesis imperfecta - shield's type ii
en Dentinogenesis imperfecta - shield's type ii (disorder)

Expression

234969005 |Dentinogenesis imperfecta - shield's type ii (disorder)|
 <<< 196286005 |Dentinogenesis imperfecta (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
3890976013 - Capdepont teeth (en) View
3890976013	en	Synonym (core metadata concept)	Capdepont teeth	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
352135019 - Dentinogenesis imperfecta without osteogenesis imperfecta (en) View
352135019	en	Synonym (core metadata concept)	Dentinogenesis imperfecta without osteogenesis imperfecta	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
352134015 - Hereditary opalescent dentine (en) View
352134015	en	Synonym (core metadata concept)	Hereditary opalescent dentine	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
352136018 - Dentinogenesis imperfecta - Shield's type II (en) View
352136018	en	Synonym (core metadata concept)	Dentinogenesis imperfecta - Shield's type II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
623358013 - Dentinogenesis imperfecta - Shield's type II (disorder) (en) View
623358013	en	Fully specified name (core metadata concept)	Dentinogenesis imperfecta - Shield's type II (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (515916025) - 234969005 -> 38199008 (363698007) View
363698007 \|Finding site (attribute)\|	38199008 \|Tooth structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6117984025) - 234969005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10517033026) - 234969005 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10517034021) - 234969005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12351256024) - 234969005 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12351257026) - 234969005 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13717832029) - 234969005 -> 84540008 (363698007) View
363698007 \|Finding site (attribute)\|	84540008 \|Dentin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4986286027) - 234969005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4986287020) - 234969005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5019651029) - 234969005 -> 38199008 (363698007) View
363698007 \|Finding site (attribute)\|	38199008 \|Tooth structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3356979022) - 234969005 -> 38199008 (363698007) View
363698007 \|Finding site (attribute)\|	38199008 \|Tooth structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3461079021) - 234969005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (515919021) - 234969005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (515920026) - 234969005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (515914027) - 234969005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (515918029) - 234969005 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1727897027) - 234969005 -> 74262004 (363698007) View
363698007 \|Finding site (attribute)\|	74262004 \|Oral cavity structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1948043023) - 234969005 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2253801025) - 234969005 -> 119253004 (363698007) View
363698007 \|Finding site (attribute)\|	119253004 \|Upper aerodigestive tract structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1727898021) - 234969005 -> 89545001 (363698007) View
363698007 \|Finding site (attribute)\|	89545001 \|Face structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (49039026) - 234969005 -> 367461002 (116680003) View
116680003 \|Is a (attribute)\|	367461002 \|Dentinogenesis imperfecta (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (515915026) - 234969005 -> 49596003 (363698007) View
363698007 \|Finding site (attribute)\|	49596003 \|Digestive organ structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (515917023) - 234969005 -> 21974007 (363698007) View
363698007 \|Finding site (attribute)\|	21974007 \|Tongue structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (515921027) - 234969005 -> 661005 (363698007) View
363698007 \|Finding site (attribute)\|	661005 \|Jaw region structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (49040029) - 234969005 -> 196286005 (116680003) View
116680003 \|Is a (attribute)\|	196286005 \|Dentinogenesis imperfecta (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
196286005 View
196286005	Dentinogenesis imperfecta (disorder)	Dentinogenesis imperfecta	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 (c9ddb9a1-0ef5-5fe5-bf36-6702b4921ac3) 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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