dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 109481002

Production

add

Component

109481002

The component that hold information about this concept.

Fully Specified Name (FSN)

Generalized enamel hypoplasia associated with fluorosis (disorder)

Shortest Term

Generalised enamel hypoplasia associated with fluorosis

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

Generalized enamel hypoplasia associated with fluorosis (disorder)

SCTID: 109481002, Primitive, Active

109481002|Generalized enamel hypoplasia associated with fluorosis (disorder)|

en Generalised enamel hypoplasia associated with fluorosis
en Generalized enamel hypoplasia associated with fluorosis
en Generalized enamel hypoplasia associated with fluorosis (disorder)

Expression

109481002 |Generalized enamel hypoplasia associated with fluorosis (disorder)|
 <<< 26597004 |Enamel hypoplasia (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 76993005 |Enamel structure (body structure)| }
        { 47429007 |Associated with (attribute)| = 244183009 |Fluorosis (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
338431015 - Generalised enamel hypoplasia associated with fluorosis (en) View
338431015	en	Synonym (core metadata concept)	Generalised enamel hypoplasia associated with fluorosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
174059014 - Generalized enamel hypoplasia associated with fluorosis (en) View
174059014	en	Synonym (core metadata concept)	Generalized enamel hypoplasia associated with fluorosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
612424012 - Generalized enamel hypoplasia associated with fluorosis (disorder) (en) View
612424012	en	Fully specified name (core metadata concept)	Generalized enamel hypoplasia associated with fluorosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (34054020) - 109481002 -> 109480001 (116680003) View
116680003 \|Is a (attribute)\|	109480001 \|Generalized enamel hypoplasia associated with systemic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2709621023) - 109481002 -> 244183009 (42752001) View
42752001 \|Due to (attribute)\|	244183009 \|Fluorosis (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12877501021) - 109481002 -> 26597004 (116680003) View
116680003 \|Is a (attribute)\|	26597004 \|Enamel hypoplasia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12877502025) - 109481002 -> 244183009 (47429007) View
47429007 \|Associated with (attribute)\|	244183009 \|Fluorosis (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1000879020) - 109481002 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1000880023) - 109481002 -> 76993005 (363698007) View
363698007 \|Finding site (attribute)\|	76993005 \|Enamel structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3322438026) - 109481002 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3322439023) - 109481002 -> 76993005 (363698007) View
363698007 \|Finding site (attribute)\|	76993005 \|Enamel structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (482683023) - 109481002 -> 661005 (363698007) View
363698007 \|Finding site (attribute)\|	661005 \|Jaw region structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
26597004 View
26597004	Enamel hypoplasia (disorder)	Enamel hypoplasia	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 (36e77060-99cd-51d4-bed1-3c035be284a2) 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)\|
ExtendedMap object (f3b646f6-ded6-56f2-8982-3bde4f9c4387) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K03.8	TRUE	ALWAYS K03.8	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)\|

Terminology chevron_right Concepts chevron_right 109481002

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches