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Terminology chevron_right Concepts chevron_right 15788006

Production

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Component

15788006

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital cleft thyroid cartilage (disorder)

Shortest Term

Khe hở sụn giáp bẩm sinh

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

Congenital cleft thyroid cartilage (disorder)

SCTID: 15788006, Defined, Active

15788006|Congenital cleft thyroid cartilage (disorder)|

vi Khe hở sụn giáp bẩm sinh
en Congenital cleft thyroid cartilage
en Congenital cleft thyroid cartilage (disorder)

Expression

15788006 |Congenital cleft thyroid cartilage (disorder)|
 === 8032007 |Congenital anomaly of thyroid cartilage (disorder)| + 
232461002 |Congenital cleft larynx (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 371520008 |Developmental failure of fusion (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 52940008 |Thyroid cartilage 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
610261000003116 - khe hở sụn giáp bẩm sinh (vi) View
610261000003116	vi	Synonym (core metadata concept)	khe hở sụn giáp bẩm sinh	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
26758014 - Congenital cleft thyroid cartilage (en) View
26758014	en	Synonym (core metadata concept)	Congenital cleft thyroid cartilage	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
742678010 - Congenital cleft thyroid cartilage (disorder) (en) View
742678010	en	Fully specified name (core metadata concept)	Congenital cleft thyroid cartilage (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11188406027) - 15788006 -> 204559005 (116680003) View
116680003 \|Is a (attribute)\|	204559005 \|Congenital fissure of larynx (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11306344025) - 15788006 -> 232461002 (116680003) View
116680003 \|Is a (attribute)\|	232461002 \|Congenital cleft larynx (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (708864027) - 15788006 -> 52940008 (363698007) View
363698007 \|Finding site (attribute)\|	52940008 \|Thyroid cartilage structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4976237022) - 15788006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4976238028) - 15788006 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4986662022) - 15788006 -> 52940008 (363698007) View
363698007 \|Finding site (attribute)\|	52940008 \|Thyroid cartilage structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5863566020) - 15788006 -> 52940008 (363698007) View
363698007 \|Finding site (attribute)\|	52940008 \|Thyroid cartilage structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6939517026) - 15788006 -> 371520008 (116676008) View
116676008 \|Associated morphology (attribute)\|	371520008 \|Developmental failure of fusion (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9536168023) - 15788006 -> 301210007 (116680003) View
116680003 \|Is a (attribute)\|	301210007 \|Lesion of larynx (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10524441028) - 15788006 -> 371520008 (116676008) View
116676008 \|Associated morphology (attribute)\|	371520008 \|Developmental failure of fusion (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10524442024) - 15788006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11188407020) - 15788006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3406728029) - 15788006 -> 4541003 (116676008) View
116676008 \|Associated morphology (attribute)\|	4541003 \|Congenital failure of fusion (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3451969020) - 15788006 -> 52940008 (363698007) View
363698007 \|Finding site (attribute)\|	52940008 \|Thyroid cartilage structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (708865026) - 15788006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2225356020) - 15788006 -> 275260000 (116680003) View
116680003 \|Is a (attribute)\|	275260000 \|Congenital malformation of the respiratory system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (708866025) - 15788006 -> 4541003 (116676008) View
116676008 \|Associated morphology (attribute)\|	4541003 \|Congenital failure of fusion (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1924831022) - 15788006 -> 113192009 (363698007) View
363698007 \|Finding site (attribute)\|	113192009 \|Skeletal system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1669475025) - 15788006 -> 67988000 (116680003) View
116680003 \|Is a (attribute)\|	67988000 \|Congenital anomaly of cartilage (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (708863022) - 15788006 -> 61496007 (363698007) View
363698007 \|Finding site (attribute)\|	61496007 \|Cartilaginous tissue structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (171763023) - 15788006 -> 8032007 (116680003) View
116680003 \|Is a (attribute)\|	8032007 \|Congenital anomaly of thyroid cartilage (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
232461002 View
232461002	Congenital cleft larynx (disorder)	Congenital cleft larynx	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
8032007 View
8032007	Congenital anomaly of thyroid cartilage (disorder)	Dị tật sụn giáp bẩm sinh	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 (5d46e5a7-90b7-54ce-9ff6-3e41d0189b43) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q31.8	TRUE	ALWAYS Q31.8	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)\|

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