dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 64971000119106

Production

add

Component

64971000119106

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of von hippel-lindau syndrome (situation)

Shortest Term

Tiền sử gia đình hội chứng von hippel-lindau

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 von hippel-lindau syndrome (situation)

SCTID: 64971000119106, Defined, Active

64971000119106|Family history of von hippel-lindau syndrome (situation)|

vi Tiền sử gia đình hội chứng von hippel-lindau
en Family history of von hippel-lindau syndrome
en Family history of von hippel-lindau syndrome (situation)

Expression

64971000119106 |Family history of von hippel-lindau syndrome (situation)|
 === 429962007 |Family history of hereditary disease (situation)| + 
297239000 |Family history of neurological disorder (situation)| + 
160288009 |Family history: neoplasm of skin (situation)| + 
160417009 |Family history: congenital anomaly (situation)| : 
        { 246090004 |Associated finding (attribute)| = 46659004 |Von hippel-lindau 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
472851000003110 - tiền sử gia đình hội chứng Von Hippel-Lindau (vi) View
472851000003110	vi	Synonym (core metadata concept)	tiền sử gia đình hội chứng Von Hippel-Lindau	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3466495016 - Family history of Von Hippel-Lindau syndrome (en) View
3466495016	en	Synonym (core metadata concept)	Family history of Von Hippel-Lindau syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3466494017 - Family history of Von Hippel-Lindau syndrome (situation) (en) View
3466494017	en	Fully specified name (core metadata concept)	Family history of Von Hippel-Lindau 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 (6968945028) - 64971000119106 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15279534024) - 64971000119106 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6968938028) - 64971000119106 -> 160406008 (116680003) View
116680003 \|Is a (attribute)\|	160406008 \|Family history: skin disease (context-dependent category)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11290545022) - 64971000119106 -> 412749001 (116680003) View
116680003 \|Is a (attribute)\|	412749001 \|Family history of development disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13647856023) - 64971000119106 -> 160288009 (116680003) View
116680003 \|Is a (attribute)\|	160288009 \|Family history: neoplasm of skin (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6968939020) - 64971000119106 -> 160417009 (116680003) View
116680003 \|Is a (attribute)\|	160417009 \|Family history: congenital anomaly (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6968940022) - 64971000119106 -> 297239000 (116680003) View
116680003 \|Is a (attribute)\|	297239000 \|Family history of neurological disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6968941021) - 64971000119106 -> 429962007 (116680003) View
116680003 \|Is a (attribute)\|	429962007 \|Family history of hereditary disease (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6968942025) - 64971000119106 -> 46659004 (246090004) View
246090004 \|Associated finding (attribute)\|	46659004 \|Von hippel-lindau syndrome (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6968943024) - 64971000119106 -> 410515003 (408729009) View
408729009 \|Finding context (attribute)\|	410515003 \|Known present (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6968944029) - 64971000119106 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (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
160288009 View
160288009	Family history: neoplasm of skin (situation)	Fh: * - skin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
297239000 View
297239000	Family history of neurological disorder (situation)	Fh: nervous system 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 (e72d6436-265d-5e68-857f-bb050d08ef58) 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)\|

Terminology chevron_right Concepts chevron_right 64971000119106

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches