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Terminology chevron_right Concepts chevron_right 64851000119105

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Language with ID “7b2ee490-b2d3-5a7d-8b27-02c6087fa615” doesn’t exist. Perhaps it was deleted?

Component

64851000119105

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of prader-willi syndrome (situation)

Shortest Term

Family history of prader-willi syndrome

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 prader-willi syndrome (situation)

SCTID: 64851000119105, Defined, Active

64851000119105|Family history of prader-willi syndrome (situation)|

vi Tiền sử gia đình mắc hội chứng prader-willi
en Family history of prader-willi syndrome
en Family history of prader-willi syndrome (situation)

Expression

64851000119105 |Family history of prader-willi syndrome (situation)|
 === 160311006 |Family history: obesity (context-dependent category)| + 
64731000119106 |Family history of multiple congenital anomalies (situation)| + 
266904009 |Family history: genitourinary disease (context-dependent category)| + 
275940001 |Family history: brain disorder (context-dependent category)| + 
160301004 |Family history of endocrine disorders (situation)| : 
        { 246090004 |Associated finding (attribute)| = 89392001 |Prader-willi 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
444691000003110 - tiền sử gia đình mắc hội chứng Prader-Willi (vi) View
444691000003110	vi	Synonym (core metadata concept)	tiền sử gia đình mắc hội chứng Prader-Willi	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3043730013 - Family history of Prader-Willi syndrome (en) View
3043730013	en	Synonym (core metadata concept)	Family history of Prader-Willi syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3043751011 - Family history of Prader-Willi syndrome (situation) (en) View
3043751011	en	Fully specified name (core metadata concept)	Family history of Prader-Willi 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 (16331371021) - 64851000119105 -> 160311006 (116680003) View
116680003 \|Is a (attribute)\|	160311006 \|Family history: obesity (context-dependent category)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054326028) - 64851000119105 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15279610023) - 64851000119105 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054324025) - 64851000119105 -> 160425006 (116680003) View
116680003 \|Is a (attribute)\|	160425006 \|Family history: chromosomal anomaly (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12088355023) - 64851000119105 -> 266904009 (116680003) View
116680003 \|Is a (attribute)\|	266904009 \|Family history: genitourinary disease (context-dependent category)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12088356024) - 64851000119105 -> 275940001 (116680003) View
116680003 \|Is a (attribute)\|	275940001 \|Family history: brain disorder (context-dependent category)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12088357026) - 64851000119105 -> 160301004 (116680003) View
116680003 \|Is a (attribute)\|	160301004 \|Family history of endocrine disorders (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6968937022) - 64851000119105 -> 64731000119106 (116680003) View
116680003 \|Is a (attribute)\|	64731000119106 \|Family history of multiple congenital anomalies (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054325029) - 64851000119105 -> 89392001 (246090004) View
246090004 \|Associated finding (attribute)\|	89392001 \|Prader-willi syndrome (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054327021) - 64851000119105 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054328027) - 64851000119105 -> 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
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
160301004 View
160301004	Family history of endocrine disorders (situation)	Fh: endocrine disorders	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160311006 View
160311006	Family history: obesity (context-dependent category)	Fh: obesity	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
266904009 View
266904009	Family history: genitourinary disease (context-dependent category)	Fh: genitourinary disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
275940001 View
275940001	Family history: brain disorder (context-dependent category)	Fh: brain disorder	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 (1db461f5-390d-546c-b463-7e77a83132bc) 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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