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Terminology chevron_right Concepts chevron_right 367461002

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Dentinogenesis imperfecta (disorder)

Shortest Term

Dentinogenesis imperfecta

Definition Status

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Dentinogenesis imperfecta (disorder)

SCTID: 367461002, Primitive, Inactive

367461002|Dentinogenesis imperfecta (disorder)|

Expression

367461002 |Dentinogenesis imperfecta (disorder)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2771347018 - Dentinogenesis imperfecta (en) View
2771347018	en	Synonym (core metadata concept)	Dentinogenesis imperfecta	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2736349010 - Dentinogenesis imperfecta (disorder) (en) View
2736349010	en	Fully specified name (core metadata concept)	Dentinogenesis imperfecta (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2670864018 - Dentinogenesis imperfecta [dup] (en) View
2670864018	en	Synonym (core metadata concept)	Dentinogenesis imperfecta [dup]	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
776167012 - Dentinogenesis imperfecta [dup] (disorder) (en) View
776167012	en	Fully specified name (core metadata concept)	Dentinogenesis imperfecta [dup] (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
492191017 - Dentinogenesis imperfecta (disorder) (en) View
492191017	en	Synonym (core metadata concept)	Dentinogenesis imperfecta (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (212602023) - 367461002 -> 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 (770984023) - 367461002 -> 661005 (363698007) View
363698007 \|Finding site (attribute)\|	661005 \|Jaw region structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (770985024) - 367461002 -> 38199008 (363698007) View
363698007 \|Finding site (attribute)\|	38199008 \|Tooth structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

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

Descriptions