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Terminology chevron_right Concepts chevron_right 71271000119107

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Component

71271000119107

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of retinitis pigmentosa (situation)

Shortest Term

Family history of retinitis pigmentosa

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 retinitis pigmentosa (situation)

SCTID: 71271000119107, Defined, Active

71271000119107|Family history of retinitis pigmentosa (situation)|

vi Tiền sử gia đình bị viêm võng mạc sắc tố
en Family history of retinitis pigmentosa
en Family history of retinitis pigmentosa (situation)

Expression

71271000119107 |Family history of retinitis pigmentosa (situation)|
 === 429962007 |Family history of hereditary disease (situation)| + 
329351000119105 |Family history of non-glaucomatous eye disorder (situation)| : 
        { 246090004 |Associated finding (attribute)| = 28835009 |Retinitis pigmentosa (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
457021000003114 - tiền sử gia đình bị viêm võng mạc sắc tố (vi) View
457021000003114	vi	Synonym (core metadata concept)	tiền sử gia đình bị viêm võng mạc sắc tố	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
2990264016 - Family history of retinitis pigmentosa (en) View
2990264016	en	Synonym (core metadata concept)	Family history of retinitis pigmentosa	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2989890016 - Family history of retinitis pigmentosa (situation) (en) View
2989890016	en	Fully specified name (core metadata concept)	Family history of retinitis pigmentosa (situation)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4960849024) - 71271000119107 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15279500023) - 71271000119107 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4960846028) - 71271000119107 -> 160346003 (116680003) View
116680003 \|Is a (attribute)\|	160346003 \|Family history: eye disorder (context-dependent category)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7116150024) - 71271000119107 -> 329351000119105 (116680003) View
116680003 \|Is a (attribute)\|	329351000119105 \|Family history of non-glaucomatous eye disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4960847021) - 71271000119107 -> 429962007 (116680003) View
116680003 \|Is a (attribute)\|	429962007 \|Family history of hereditary disease (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4960848027) - 71271000119107 -> 28835009 (246090004) View
246090004 \|Associated finding (attribute)\|	28835009 \|Retinitis pigmentosa (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4960850024) - 71271000119107 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4960851023) - 71271000119107 -> 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
329351000119105 View
329351000119105	Family history of non-glaucomatous eye disorder (situation)	Family history of non-glaucomatous eye disorder	900000000000074008 \|Necessary but not sufficient concept 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

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 (c918ba70-0225-5120-ab8a-c1097ae2e37e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.5	TRUE	ALWAYS Z83.5	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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