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Terminology chevron_right Concepts chevron_right 64161000119102

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Component

64161000119102

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of phenylketonuria (situation)

Shortest Term

Family history of phenylketonuria

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 phenylketonuria (situation)

SCTID: 64161000119102, Defined, Active

64161000119102|Family history of phenylketonuria (situation)|

vi Tiền sử gia đình mắc phenylketon niệu
en Family history of phenylketonuria
en Family history of phenylketonuria (situation)

Expression

64161000119102 |Family history of phenylketonuria (situation)|
 === 160417009 |Family history: congenital anomaly (situation)| + 
160305008 |Family history of metabolic disorder (situation)| + 
429962007 |Family history of hereditary disease (situation)| : 
        { 246090004 |Associated finding (attribute)| = 7573000 |Classical phenylketonuria (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
441171000003116 - tiền sử gia đình mắc phenylketon niệu (vi) View
441171000003116	vi	Synonym (core metadata concept)	tiền sử gia đình mắc phenylketon niệu	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3043581018 - Family history of phenylketonuria (en) View
3043581018	en	Synonym (core metadata concept)	Family history of phenylketonuria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3043641019 - Family history of phenylketonuria (situation) (en) View
3043641019	en	Fully specified name (core metadata concept)	Family history of phenylketonuria (situation)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6054334023) - 64161000119102 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15279601026) - 64161000119102 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054330025) - 64161000119102 -> 160417009 (116680003) View
116680003 \|Is a (attribute)\|	160417009 \|Family history: congenital anomaly (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054331026) - 64161000119102 -> 160305008 (116680003) View
116680003 \|Is a (attribute)\|	160305008 \|Family history of metabolic disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054332022) - 64161000119102 -> 429962007 (116680003) View
116680003 \|Is a (attribute)\|	429962007 \|Family history of hereditary disease (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054333028) - 64161000119102 -> 7573000 (246090004) View
246090004 \|Associated finding (attribute)\|	7573000 \|Classical phenylketonuria (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054335024) - 64161000119102 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054336020) - 64161000119102 -> 410515003 (408729009) View
408729009 \|Finding context (attribute)\|	410515003 \|Known present (qualifier value)\|	1	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
160305008 View
160305008	Family history of metabolic disorder (situation)	Fh: metabolic 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 (d52b6560-0b8b-59ae-afe1-71ffc569674d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.4	TRUE	ALWAYS Z83.4	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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