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Terminology chevron_right Concepts chevron_right 98251000119101

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Extended Map with ID “17659d55-4e14-5e8f-b5a9-b1a7274dcfb0” doesn’t exist. Perhaps it was deleted?

Component

98251000119101

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of spongy degeneration of central nervous system (situation)

Shortest Term

Family history of canavan disease

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 spongy degeneration of central nervous system (situation)

SCTID: 98251000119101, Defined, Active

98251000119101|Family history of spongy degeneration of central nervous system (situation)|

vi Bệnh canavan (bệnh di truyền gen lặn gây tổn thương tiến triển tế bào thần kinh trong não phổ biến ở trẻ sơ sinh) có tiền sử gia đình
en Family history of canavan disease
en Family history of spongy degeneration of central nervous system
en Family history of spongy degeneration of central nervous system (situation)

Expression

98251000119101 |Family history of spongy degeneration of central nervous system (situation)|
 === 160305008 |Family history of metabolic disorder (situation)| + 
266891008 |Family history of central nervous system disorder (situation)| + 
430814002 |Family history of neuropathy (situation)| + 
429962007 |Family history of hereditary disease (situation)| : 
        { 246090004 |Associated finding (attribute)| = 80544005 |Spongy degeneration of central nervous system (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
449291000003113 - bệnh Canavan (bệnh di truyền gen lặn gây tổn thương tiến triển tế bào thần kinh trong não phổ biến ở trẻ sơ sinh) có tiền sử gia đình (vi) View
449291000003113	vi	Synonym (core metadata concept)	bệnh Canavan (bệnh di truyền gen lặn gây tổn thương tiến triển tế bào thần kinh trong não phổ biến ở trẻ sơ sinh) có tiền sử gia đình	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3042592013 - Family history of Canavan disease (en) View
3042592013	en	Synonym (core metadata concept)	Family history of Canavan disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3042998019 - Family history of spongy degeneration of central nervous system (en) View
3042998019	en	Synonym (core metadata concept)	Family history of spongy degeneration of central nervous system	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3043714017 - Family history of spongy degeneration of central nervous system (situation) (en) View
3043714017	en	Fully specified name (core metadata concept)	Family history of spongy degeneration of central nervous system (situation)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15587927023) - 98251000119101 -> 430814002 (116680003) View
116680003 \|Is a (attribute)\|	430814002 \|Family history of neuropathy (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15588455027) - 98251000119101 -> 429962007 (116680003) View
116680003 \|Is a (attribute)\|	429962007 \|Family history of hereditary disease (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6046107020) - 98251000119101 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15279630022) - 98251000119101 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6046104029) - 98251000119101 -> 160305008 (116680003) View
116680003 \|Is a (attribute)\|	160305008 \|Family history of metabolic disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6046105028) - 98251000119101 -> 266891008 (116680003) View
116680003 \|Is a (attribute)\|	266891008 \|Family history of central nervous system disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6046106027) - 98251000119101 -> 80544005 (246090004) View
246090004 \|Associated finding (attribute)\|	80544005 \|Spongy degeneration of central nervous system (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6046108026) - 98251000119101 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6046109023) - 98251000119101 -> 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
430814002 View
430814002	Family history of neuropathy (situation)	Family history of neuropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
266891008 View
266891008	Family history of central nervous system disorder (situation)	Fh: cns disorder	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

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 (90a34509-8105-549b-9195-b644550fab24) 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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