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Terminology chevron_right Concepts chevron_right 65021000119105

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Language with ID “8305a9b7-83e8-540c-81a2-b4f97b764920” doesn’t exist. Perhaps it was deleted?

Component

65021000119105

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of neurofibromatosis (situation)

Shortest Term

Tiền sử gia đình u xơ thần kinh

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 neurofibromatosis (situation)

SCTID: 65021000119105, Defined, Active

65021000119105|Family history of neurofibromatosis (situation)|

vi Tiền sử gia đình u xơ thần kinh
en Family history of neurofibromatosis
en Family history of neurofibromatosis (situation)

Expression

65021000119105 |Family history of neurofibromatosis (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)| = 19133005 |Neurofibromatosis 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
472801000003114 - tiền sử gia đình u xơ thần kinh (vi) View
472801000003114	vi	Synonym (core metadata concept)	tiền sử gia đình u xơ thần kinh	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3043725014 - Family history of neurofibromatosis (en) View
3043725014	en	Synonym (core metadata concept)	Family history of neurofibromatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3043643016 - Family history of neurofibromatosis (situation) (en) View
3043643016	en	Fully specified name (core metadata concept)	Family history of neurofibromatosis (situation)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6054431027) - 65021000119105 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15279614025) - 65021000119105 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11290534024) - 65021000119105 -> 412749001 (116680003) View
116680003 \|Is a (attribute)\|	412749001 \|Family history of development disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6054426029) - 65021000119105 -> 160406008 (116680003) View
116680003 \|Is a (attribute)\|	160406008 \|Family history: skin disease (context-dependent category)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6054428028) - 65021000119105 -> 429962007 (116680003) View
116680003 \|Is a (attribute)\|	429962007 \|Family history of hereditary disease (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12088358020) - 65021000119105 -> 160288009 (116680003) View
116680003 \|Is a (attribute)\|	160288009 \|Family history: neoplasm of skin (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054427022) - 65021000119105 -> 266883004 (116680003) View
116680003 \|Is a (attribute)\|	266883004 \|Family history of neoplasm (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6054425025) - 65021000119105 -> 160417009 (116680003) View
116680003 \|Is a (attribute)\|	160417009 \|Family history: congenital anomaly (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054429020) - 65021000119105 -> 297239000 (116680003) View
116680003 \|Is a (attribute)\|	297239000 \|Family history of neurological disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054430026) - 65021000119105 -> 19133005 (246090004) View
246090004 \|Associated finding (attribute)\|	19133005 \|Neurofibromatosis syndrome (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054432023) - 65021000119105 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6054433029) - 65021000119105 -> 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
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 (96bb65bd-4262-5c6c-8051-0a078d780a10) 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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