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Terminology chevron_right Concepts chevron_right 196279002

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Component

196279002

The component that hold information about this concept.

Fully Specified Name (FSN)

Neonatal enamel hypoplasia (disorder)

Shortest Term

Neonatal enamel hypoplasia

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

Neonatal enamel hypoplasia (disorder)

SCTID: 196279002, Defined, Active

196279002|Neonatal enamel hypoplasia (disorder)|

en Neonatal enamel hypoplasia
en Neonatal enamel hypoplasia (disorder)

Expression

196279002 |Neonatal enamel hypoplasia (disorder)|
 === 42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| + 
108111000119103 |Acquired anomaly of mouth (disorder)| + 
22925008 |Neonatal disorder (disorder)| + 
26597004 |Enamel hypoplasia (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 76993005 |Enamel structure (body structure)|,
246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
301903014 - Neonatal enamel hypoplasia (en) View
301903014	en	Synonym (core metadata concept)	Neonatal enamel hypoplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
580490010 - Neonatal enamel hypoplasia (disorder) (en) View
580490010	en	Fully specified name (core metadata concept)	Neonatal enamel hypoplasia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9656890027) - 196279002 -> 42357009 (116680003) View
116680003 \|Is a (attribute)\|	42357009 \|Disorder of digestive system specific to fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2742866026) - 196279002 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12921170023) - 196279002 -> 108111000119103 (116680003) View
116680003 \|Is a (attribute)\|	108111000119103 \|Acquired anomaly of mouth (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12921171022) - 196279002 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (962657025) - 196279002 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (962658024) - 196279002 -> 76993005 (363698007) View
363698007 \|Finding site (attribute)\|	76993005 \|Enamel structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3303073020) - 196279002 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3303074025) - 196279002 -> 76993005 (363698007) View
363698007 \|Finding site (attribute)\|	76993005 \|Enamel structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2700426029) - 196279002 -> 22925008 (116680003) View
116680003 \|Is a (attribute)\|	22925008 \|Neonatal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (962656023) - 196279002 -> 661005 (363698007) View
363698007 \|Finding site (attribute)\|	661005 \|Jaw region structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (327655023) - 196279002 -> 26597004 (116680003) View
116680003 \|Is a (attribute)\|	26597004 \|Enamel hypoplasia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
108111000119103 View
108111000119103	Acquired anomaly of mouth (disorder)	Acquired anomaly of mouth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
42357009 View
42357009	Disorder of digestive system specific to fetus or newborn (disorder)	Perinatal digestive system disorders	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
26597004 View
26597004	Enamel hypoplasia (disorder)	Enamel hypoplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
22925008 View
22925008	Neonatal disorder (disorder)	Neonatal disease	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 (10fb0e8d-b60c-5c31-9c4d-a8048d146780) 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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