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Terminology chevron_right Concepts chevron_right 725052002

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Component

725052002

The component that hold information about this concept.

Fully Specified Name (FSN)

Fetal cystic fibrosis (disorder)

Shortest Term

Xơ nang bào thai

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

Fetal cystic fibrosis (disorder)

SCTID: 725052002, Defined, Active

725052002|Fetal cystic fibrosis (disorder)|

vi Xơ nang bào thai
en Fetal cystic fibrosis
en Fetal cystic fibrosis (disorder)
en Foetal cystic fibrosis

Expression

725052002 |Fetal cystic fibrosis (disorder)|
 === 190905008 |Cystic fibrosis (disorder)| + 
199531009 |Fetal hereditary disease (disorder)| : 
        { 363698007 |Finding site (attribute)| = 321667001 |Respiratory tract structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
363714003 |Interprets (attribute)| = 63533009 |Mucociliary clearance, function (observable entity)| }
        { 246454002 |Occurrence (attribute)| = 303112003 |Fetal period (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
486011000003110 - Xơ nang bào thai (vi) View
486011000003110	vi	Synonym (core metadata concept)	Xơ nang bào thai	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3437591013 - Fetal cystic fibrosis (en) View
3437591013	en	Synonym (core metadata concept)	Fetal cystic fibrosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3437590014 - Fetal cystic fibrosis (disorder) (en) View
3437590014	en	Fully specified name (core metadata concept)	Fetal cystic fibrosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3437592018 - Foetal cystic fibrosis (en) View
3437592018	en	Synonym (core metadata concept)	Foetal cystic fibrosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (7341349022) - 725052002 -> 6920004 (116676008) View
116676008 \|Associated morphology (attribute)\|	6920004 \|Defect (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6874760027) - 725052002 -> 70591005 (116680003) View
116680003 \|Is a (attribute)\|	70591005 \|Fetal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15230738020) - 725052002 -> 199531009 (116680003) View
116680003 \|Is a (attribute)\|	199531009 \|Fetal hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6874762024) - 725052002 -> 303112003 (246454002) View
246454002 \|Occurrence (attribute)\|	303112003 \|Fetal period (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7341350022) - 725052002 -> 321667001 (363698007) View
363698007 \|Finding site (attribute)\|	321667001 \|Respiratory tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7341351021) - 725052002 -> 260379002 (363713009) View
363713009 \|Has interpretation (attribute)\|	260379002 \|Impaired (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7341352025) - 725052002 -> 63533009 (363714003) View
363714003 \|Interprets (attribute)\|	63533009 \|Mucociliary clearance, function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6874761028) - 725052002 -> 190905008 (116680003) View
116680003 \|Is a (attribute)\|	190905008 \|Cystic fibrosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
199531009 View
199531009	Fetal hereditary disease (disorder)	Fetal hereditary disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
190905008 View
190905008	Cystic fibrosis (disorder)	Cf	900000000000074008 \|Necessary but not sufficient concept 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 (b57bdab7-52a6-54b8-8cbe-72ebe2e0bb13) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E84.9	TRUE	ALWAYS E84.9	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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