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Terminology chevron_right Concepts chevron_right 190905008

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Component

190905008

The component that hold information about this concept.

Fully Specified Name (FSN)

Cystic fibrosis (disorder)

Shortest Term

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Cystic fibrosis (disorder)

SCTID: 190905008, Primitive, Active

190905008|Cystic fibrosis (disorder)|

vi Bệnh xơ nang
vi Bệnh xơ nang
en Cystic fibrosis
en Cystic fibrosis (disorder)
en Fibrocystic disease
en Mucoviscidosis
en Cf - cystic fibrosis

Expression

190905008 |Cystic fibrosis (disorder)|
 <<< 233661002 |Inherited mucociliary clearance defect (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
363714003 |Interprets (attribute)| = 63533009 |Mucociliary clearance, function (observable entity)| }
        { 363698007 |Finding site (attribute)| = 321667001 |Respiratory tract structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
597701000003119 - bệnh xơ nang (vi) View
597701000003119	vi	Synonym (core metadata concept)	bệnh xơ nang	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
566431000003118 - bệnh xơ nang (vi) View
566431000003118	vi	Synonym (core metadata concept)	bệnh xơ nang	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
293531018 - CF (en) View
293531018	en	Synonym (core metadata concept)	CF	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
293528019 - Cystic fibrosis (en) View
293528019	en	Synonym (core metadata concept)	Cystic fibrosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
574544017 - Cystic fibrosis (disorder) (en) View
574544017	en	Fully specified name (core metadata concept)	Cystic fibrosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
293530017 - Fibrocystic disease (en) View
293530017	en	Synonym (core metadata concept)	Fibrocystic disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
293532013 - Mucoviscidosis (en) View
293532013	en	Synonym (core metadata concept)	Mucoviscidosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
293529010 - CF - Cystic fibrosis (en) View
293529010	en	Synonym (core metadata concept)	CF - Cystic fibrosis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (7341027023) - 190905008 -> 6920004 (116676008) View
116676008 \|Associated morphology (attribute)\|	6920004 \|Defect (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12252217027) - 190905008 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7341025026) - 190905008 -> 260379002 (363713009) View
363713009 \|Has interpretation (attribute)\|	260379002 \|Impaired (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7341026025) - 190905008 -> 63533009 (363714003) View
363714003 \|Interprets (attribute)\|	63533009 \|Mucociliary clearance, function (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7341028029) - 190905008 -> 321667001 (363698007) View
363698007 \|Finding site (attribute)\|	321667001 \|Respiratory tract structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (19287022) - 190905008 -> 50043002 (116680003) View
116680003 \|Is a (attribute)\|	50043002 \|Disorder of respiratory system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (462448022) - 190905008 -> 20139000 (363698007) View
363698007 \|Finding site (attribute)\|	20139000 \|Structure of respiratory system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (19288028) - 190905008 -> 233661002 (116680003) View
116680003 \|Is a (attribute)\|	233661002 \|Inherited mucociliary clearance defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
233661002 View
233661002	Inherited mucociliary clearance defect (disorder)	Inherited mucociliary clearance defect	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1296527009 View
1296527009	Cystic fibrosis due to heterozygous deltaf508 mutation (disorder)	Deltaf508 heterozygous mucoviscidosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1296528004 View
1296528004	Cystic fibrosis due to homozygous deltaf508 mutation (disorder)	Deltaf508 homozygous mucoviscidosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
762269004 View
762269004	Classical cystic fibrosis (disorder)	Bệnh xơ nang kinh điển	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
762270003 View
762270003	Atypical cystic fibrosis (disorder)	Atypical cystic fibrosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
762271004 View
762271004	Subclinical cystic fibrosis (disorder)	Bệnh xơ nang tiền lâm sàng	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
725052002 View
725052002	Fetal cystic fibrosis (disorder)	Xơ nang bào thai	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
720401009 View
720401009	Cystic fibrosis with gastritis and megaloblastic anemia syndrome (disorder)	Lubani al-saleh teebi syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
235978006 View
235978006	Cystic fibrosis of pancreas (disorder)	Xơ nang tụy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
716088000 View
716088000	Follicular hamartoma with alopecia and cystic fibrosis syndrome (disorder)	U mô thừa dạng nang với rụng tóc và hội chứng xơ nang	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
427089005 View
427089005	Diabetes mellitus due to cystic fibrosis (disorder)	Diabetes mellitus due to cystic fibrosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
81423003 View
81423003	Cystic fibrosis without meconium ileus (disorder)	Bệnh xơ nang không do phân su	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
86092005 View
86092005	Cystic fibrosis with meconium ileus (disorder)	Meconium ileus	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
86555001 View
86555001	Cystic fibrosis of the lung (disorder)	Bệnh xơ nang phổi	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (05dfc7ca-a186-5cef-9cfd-b8032133eadb) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E84.0	IFA 86555001 \| Cystic fibrosis of the lung (disorder) \|	IF CYSTIC FIBROSIS OF THE LUNG CHOOSE E84.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (3d787145-f593-57e8-b9dc-2462ca25c4de) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P75	IFA 86092005 \| Cystic fibrosis with meconium ileus (disorder) \|	IF CYSTIC FIBROSIS WITH MECONIUM ILEUS CHOOSE P75 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (48534214-510d-51dd-a0dd-2472f111fcd9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E84.9	OTHERWISE 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)\|
ExtendedMap object (6690b58c-542d-555e-907d-c400fa15d4be) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E84.1	IFA 86092005 \| Cystic fibrosis with meconium ileus (disorder) \|	IF CYSTIC FIBROSIS WITH MECONIUM ILEUS CHOOSE E84.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (a7213a9a-8f26-51c8-a52f-3bd6797201f2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (c9a1e6d0-99a7-5e98-ad84-059b5250f17b) 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)\|
ExtendedMap object (e9282039-328c-5d00-b96e-44f0a93b3485) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E84.1	IFA 190909002 \| Cystic fibrosis with intestinal manifestations (disorder) \|	IF CYSTIC FIBROSIS WITH INTESTINAL MANIFESTATIONS CHOOSE E84.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (05dfc7ca-a186-5cef-9cfd-b8032133eadb) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E84.0	IFA 86555001 \| Cystic fibrosis of the lung (disorder) \|	IF CYSTIC FIBROSIS OF THE LUNG CHOOSE E84.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (3d787145-f593-57e8-b9dc-2462ca25c4de) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P75	IFA 86092005 \| Cystic fibrosis with meconium ileus (disorder) \|	IF CYSTIC FIBROSIS WITH MECONIUM ILEUS CHOOSE P75 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (48534214-510d-51dd-a0dd-2472f111fcd9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E84.9	OTHERWISE 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)\|
ExtendedMap object (6690b58c-542d-555e-907d-c400fa15d4be) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E84.1	IFA 86092005 \| Cystic fibrosis with meconium ileus (disorder) \|	IF CYSTIC FIBROSIS WITH MECONIUM ILEUS CHOOSE E84.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (a7213a9a-8f26-51c8-a52f-3bd6797201f2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (c9a1e6d0-99a7-5e98-ad84-059b5250f17b) 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)\|
ExtendedMap object (e9282039-328c-5d00-b96e-44f0a93b3485) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E84.1	IFA 190909002 \| Cystic fibrosis with intestinal manifestations (disorder) \|	IF CYSTIC FIBROSIS WITH INTESTINAL MANIFESTATIONS CHOOSE E84.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

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