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Terminology chevron_right Concepts chevron_right 699382004

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Component

699382004

The component that hold information about this concept.

Fully Specified Name (FSN)

Agenesis of enamel (disorder)

Shortest Term

Enamel agenesis

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

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

Summary

Agenesis of enamel (disorder)

SCTID: 699382004, Defined, Active

699382004|Agenesis of enamel (disorder)|

en Agenesis of enamel
en Agenesis of enamel (disorder)
en Enamel agenesis

Expression

699382004 |Agenesis of enamel (disorder)|
 === 78494001 |Amelogenesis imperfecta (disorder)| + 
91946007 |Congenital absence of mouth (disorder)| + 
91922000 |Congenital absence of jaw (disorder)| + 
234951001 |Developmental absence of tooth (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 782173000 |Agenesis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 362113009 |Entire enamel (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
4552522011 - Agenesis of enamel (en) View
4552522011	en	Synonym (core metadata concept)	Agenesis of enamel	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4552523018 - Agenesis of enamel (disorder) (en) View
4552523018	en	Fully specified name (core metadata concept)	Agenesis of enamel (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2984313014 - Enamel agenesis (disorder) (en) View
2984313014	en	Fully specified name (core metadata concept)	Enamel agenesis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	False
2984366012 - Enamel agenesis (en) View
2984366012	en	Synonym (core metadata concept)	Enamel agenesis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13883136022) - 699382004 -> 234951001 (116680003) View
116680003 \|Is a (attribute)\|	234951001 \|Developmental absence of tooth (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5000490024) - 699382004 -> 76993005 (363698007) View
363698007 \|Finding site (attribute)\|	76993005 \|Enamel structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11151313026) - 699382004 -> 45486003 (116676008) View
116676008 \|Associated morphology (attribute)\|	45486003 \|Aplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13724280026) - 699382004 -> 782173000 (116676008) View
116676008 \|Associated morphology (attribute)\|	782173000 \|Agenesis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13724293020) - 699382004 -> 362113009 (363698007) View
363698007 \|Finding site (attribute)\|	362113009 \|Entire enamel (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5000486022) - 699382004 -> 91946007 (116680003) View
116680003 \|Is a (attribute)\|	91946007 \|Congenital absence of mouth (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5000488023) - 699382004 -> 91922000 (116680003) View
116680003 \|Is a (attribute)\|	91922000 \|Congenital absence of jaw (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11187473021) - 699382004 -> 83028006 (116680003) View
116680003 \|Is a (attribute)\|	83028006 \|Congenital partial absence of alimentary tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000489026) - 699382004 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10522076020) - 699382004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4778545024) - 699382004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4778546020) - 699382004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4778547027) - 699382004 -> 76993005 (363698007) View
363698007 \|Finding site (attribute)\|	76993005 \|Enamel structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4778548021) - 699382004 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4778549029) - 699382004 -> 76993005 (363698007) View
363698007 \|Finding site (attribute)\|	76993005 \|Enamel structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989760024) - 699382004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4778544023) - 699382004 -> 78494001 (116680003) View
116680003 \|Is a (attribute)\|	78494001 \|Amelogenesis imperfecta (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
234951001 View
234951001	Developmental absence of tooth (disorder)	Developmental absence of tooth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
78494001 View
78494001	Amelogenesis imperfecta (disorder)	Amelogenesis imperfecta	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
91922000 View
91922000	Congenital absence of jaw (disorder)	Agnathia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
91946007 View
91946007	Congenital absence of mouth (disorder)	Astomia	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 (861db484-6c71-504d-8270-e04cf9072967) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K00.4	TRUE	ALWAYS K00.4	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)\|

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