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Terminology chevron_right Concepts chevron_right 64251000119106

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Component

64251000119106

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of glycogen storage disease (situation)

Shortest Term

Tiền sử gia đình mắc bệnh dự trữ glycogen

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 glycogen storage disease (situation)

SCTID: 64251000119106, Defined, Active

64251000119106|Family history of glycogen storage disease (situation)|

vi Tiền sử gia đình mắc bệnh dự trữ glycogen
en Family history of glycogen storage disease
en Family history of glycogen storage disease (situation)

Expression

64251000119106 |Family history of glycogen storage disease (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)| = 29633007 |Glycogen storage disease (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
441151000003112 - tiền sử gia đình mắc bệnh dự trữ glycogen (vi) View
441151000003112	vi	Synonym (core metadata concept)	tiền sử gia đình mắc bệnh dự trữ glycogen	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3042902012 - Family history of glycogen storage disease (en) View
3042902012	en	Synonym (core metadata concept)	Family history of glycogen storage disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3042898018 - Family history of glycogen storage disease (situation) (en) View
3042898018	en	Fully specified name (core metadata concept)	Family history of glycogen storage disease (situation)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6047531026) - 64251000119106 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15279603028) - 64251000119106 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6047527021) - 64251000119106 -> 160417009 (116680003) View
116680003 \|Is a (attribute)\|	160417009 \|Family history: congenital anomaly (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6047528027) - 64251000119106 -> 160305008 (116680003) View
116680003 \|Is a (attribute)\|	160305008 \|Family history of metabolic disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6047529024) - 64251000119106 -> 429962007 (116680003) View
116680003 \|Is a (attribute)\|	429962007 \|Family history of hereditary disease (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6047530025) - 64251000119106 -> 29633007 (246090004) View
246090004 \|Associated finding (attribute)\|	29633007 \|Glycogen storage disease (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6047532022) - 64251000119106 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6047533028) - 64251000119106 -> 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 (019d650f-4a68-52d1-af25-c02af364f913) 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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