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Terminology chevron_right Concepts chevron_right 417001009

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Component

417001009

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of tuberous sclerosis (situation)

Shortest Term

Family history of tuberous sclerosis

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 tuberous sclerosis (situation)

SCTID: 417001009, Defined, Active

417001009|Family history of tuberous sclerosis (situation)|

vi Tiền sử gia đình bệnh xơ cứng dạng củ
en Family history of tuberous sclerosis
en Family history of tuberous sclerosis (situation)

Expression

417001009 |Family history of tuberous sclerosis (situation)|
 === 160417009 |Family history: congenital anomaly (situation)| + 
429962007 |Family history of hereditary disease (situation)| + 
160288009 |Family history: neoplasm of skin (situation)| + 
266891008 |Family history of central nervous system disorder (situation)| : 
        { 246090004 |Associated finding (attribute)| = 7199000 |Tuberous sclerosis 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
475521000003111 - tiền sử gia đình bệnh xơ cứng dạng củ (vi) View
475521000003111	vi	Synonym (core metadata concept)	tiền sử gia đình bệnh xơ cứng dạng củ	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
2549545018 - Family history of tuberous sclerosis (en) View
2549545018	en	Synonym (core metadata concept)	Family history of tuberous sclerosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2613604019 - Family history of tuberous sclerosis (situation) (en) View
2613604019	en	Fully specified name (core metadata concept)	Family history of tuberous sclerosis (situation)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2547211017 - Family history of tuberous sclerosis (context-dependent category) (en) View
2547211017	en	Fully specified name (core metadata concept)	Family history of tuberous sclerosis (context-dependent category)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3522430028) - 417001009 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3789185025) - 417001009 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2776226026) - 417001009 -> 160406008 (116680003) View
116680003 \|Is a (attribute)\|	160406008 \|Family history: skin disease (context-dependent category)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2776228025) - 417001009 -> 297239000 (116680003) View
116680003 \|Is a (attribute)\|	297239000 \|Family history of neurological disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11290852026) - 417001009 -> 412749001 (116680003) View
116680003 \|Is a (attribute)\|	412749001 \|Family history of development disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13647805025) - 417001009 -> 160288009 (116680003) View
116680003 \|Is a (attribute)\|	160288009 \|Family history: neoplasm of skin (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13798200029) - 417001009 -> 266891008 (116680003) View
116680003 \|Is a (attribute)\|	266891008 \|Family history of central nervous system disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3522431029) - 417001009 -> 410515003 (408729009) View
408729009 \|Finding context (attribute)\|	410515003 \|Known present (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3522433026) - 417001009 -> 7199000 (246090004) View
246090004 \|Associated finding (attribute)\|	7199000 \|Tuberous sclerosis syndrome (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3652657021) - 417001009 -> 410515003 (408729009) View
408729009 \|Finding context (attribute)\|	410515003 \|Known present (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3693933022) - 417001009 -> 7199000 (246090004) View
246090004 \|Associated finding (attribute)\|	7199000 \|Tuberous sclerosis syndrome (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3693934027) - 417001009 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3693935026) - 417001009 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3780398021) - 417001009 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3522432020) - 417001009 -> 410512000 (408731000) View
408731000 \|Temporal context (attribute)\|	410512000 \|Current or specified time (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2796909021) - 417001009 -> 410512000 (408731000) View
408731000 \|Temporal context (attribute)\|	410512000 \|Current or specified time (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2796910027) - 417001009 -> 410515003 (408729009) View
408729009 \|Finding context (attribute)\|	410515003 \|Known present (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2796911028) - 417001009 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2796912024) - 417001009 -> 7199000 (246090004) View
246090004 \|Associated finding (attribute)\|	7199000 \|Tuberous sclerosis syndrome (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3271083023) - 417001009 -> 429962007 (116680003) View
116680003 \|Is a (attribute)\|	429962007 \|Family history of hereditary disease (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2776227024) - 417001009 -> 160417009 (116680003) View
116680003 \|Is a (attribute)\|	160417009 \|Family history: congenital anomaly (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
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
160288009 View
160288009	Family history: neoplasm of skin (situation)	Fh: * - skin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
266891008 View
266891008	Family history of central nervous system disorder (situation)	Fh: cns disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160417009 View
160417009	Family history: congenital anomaly (situation)	Fh: congenital 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 (3501b01a-4d21-5432-a472-e387fb966afa) 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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