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Terminology chevron_right Concepts chevron_right 65031000119108

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Component

65031000119108

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of cowden syndrome (situation)

Shortest Term

Tiền sử gia đình hội chứng cowden

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

Family history of cowden syndrome (situation)

SCTID: 65031000119108, Defined, Active

65031000119108|Family history of cowden syndrome (situation)|

vi Tiền sử gia đình hội chứng cowden
en Family history of cowden syndrome
en Family history of cowden syndrome (situation)

Expression

65031000119108 |Family history of cowden syndrome (situation)|
 === 429962007 |Family history of hereditary disease (situation)| + 
160406008 |Family history: skin disease (context-dependent category)| + 
64731000119106 |Family history of multiple congenital anomalies (situation)| + 
160422009 |Family history: congenital gastrointestinal tract anomaly (context-dependent category)| : 
        { 246090004 |Associated finding (attribute)| = 58037000 |Cowden syndrome (disorder)|,
408729009 |Finding context (attribute)| = 410515003 |Known present (qualifier value)|,
408732007 |Subject relationship context (attribute)| = 303071001 |Person in the family (person)|,
408731000 |Temporal context (attribute)| = 410511007 |Current or past (actual) (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
472791000003110 - tiền sử gia đình hội chứng Cowden (vi) View
472791000003110	vi	Synonym (core metadata concept)	tiền sử gia đình hội chứng Cowden	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3438377016 - Family history of Cowden syndrome (en) View
3438377016	en	Synonym (core metadata concept)	Family history of Cowden syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3438376013 - Family history of Cowden syndrome (situation) (en) View
3438376013	en	Fully specified name (core metadata concept)	Family history of Cowden syndrome (situation)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6876355025) - 65031000119108 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15279535020) - 65031000119108 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6876348027) - 65031000119108 -> 160381001 (116680003) View
116680003 \|Is a (attribute)\|	160381001 \|Family history: gastrointestinal disease (context-dependent category)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10534426022) - 65031000119108 -> 160422009 (116680003) View
116680003 \|Is a (attribute)\|	160422009 \|Family history: congenital gastrointestinal tract anomaly (context-dependent category)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6876349024) - 65031000119108 -> 160417009 (116680003) View
116680003 \|Is a (attribute)\|	160417009 \|Family history: congenital anomaly (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6876350024) - 65031000119108 -> 266883004 (116680003) View
116680003 \|Is a (attribute)\|	266883004 \|Family history of neoplasm (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9160186025) - 65031000119108 -> 160406008 (116680003) View
116680003 \|Is a (attribute)\|	160406008 \|Family history: skin disease (context-dependent category)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9160187023) - 65031000119108 -> 64731000119106 (116680003) View
116680003 \|Is a (attribute)\|	64731000119106 \|Family history of multiple congenital anomalies (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6876351023) - 65031000119108 -> 429962007 (116680003) View
116680003 \|Is a (attribute)\|	429962007 \|Family history of hereditary disease (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6876352027) - 65031000119108 -> 58037000 (246090004) View
246090004 \|Associated finding (attribute)\|	58037000 \|Cowden syndrome (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6876353021) - 65031000119108 -> 410515003 (408729009) View
408729009 \|Finding context (attribute)\|	410515003 \|Known present (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6876354026) - 65031000119108 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
64731000119106 View
64731000119106	Family history of multiple congenital anomalies (situation)	Tiền sử gia đình đa dị tật bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
429962007 View
429962007	Family history of hereditary disease (situation)	Family history of genetic disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160406008 View
160406008	Family history: skin disease (context-dependent category)	Fh: skin disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160422009 View
160422009	Family history: congenital gastrointestinal tract anomaly (context-dependent category)	Fh: congenital git anomaly	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 (3f14c8a9-9d78-5b3a-bbd9-fd657d545246) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z82.7	TRUE	ALWAYS Z82.7	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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