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Terminology chevron_right Concepts chevron_right 19346006

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Component

19346006

The component that hold information about this concept.

Fully Specified Name (FSN)

Marfan's syndrome (disorder)

Shortest Term

Marfan syndrome

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

Marfan's syndrome (disorder)

SCTID: 19346006, Primitive, Active

19346006|Marfan's syndrome (disorder)|

vi Hội chứng marfan
en Marfan syndrome
en Marfan's syndrome (disorder)
en Marfan's disease
en Marfan's syndrome

Expression

19346006 |Marfan's syndrome (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
363045008 |Connective tissue hereditary disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 21793004 |Connective tissue structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
597271000003116 - hội chứng Marfan (vi) View
597271000003116	vi	Synonym (core metadata concept)	hội chứng Marfan	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2839233010 - Marfan syndrome (en) View
2839233010	en	Synonym (core metadata concept)	Marfan syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
747367019 - Marfan's syndrome (disorder) (en) View
747367019	en	Fully specified name (core metadata concept)	Marfan's syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
32613016 - Marfan's disease (en) View
32613016	en	Synonym (core metadata concept)	Marfan's disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
32612014 - Marfan's syndrome (en) View
32612014	en	Synonym (core metadata concept)	Marfan's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2591953028) - 19346006 -> 21793004 (363698007) View
363698007 \|Finding site (attribute)\|	21793004 \|Connective tissue structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (178480029) - 19346006 -> 240259000 (116680003) View
116680003 \|Is a (attribute)\|	240259000 \|Inherited disorder of connective tissue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6026394021) - 19346006 -> 363045008 (116680003) View
116680003 \|Is a (attribute)\|	363045008 \|Connective tissue hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2484245024) - 19346006 -> 257728006 (363698007) View
363698007 \|Finding site (attribute)\|	257728006 \|Anatomical concepts (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1759266025) - 19346006 -> 91723000 (363698007) View
363698007 \|Finding site (attribute)\|	91723000 \|Anatomical structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (719458028) - 19346006 -> 181769001 (363698007) View
363698007 \|Finding site (attribute)\|	181769001 \|Connective tissue (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (719459020) - 19346006 -> 26107004 (363698007) View
363698007 \|Finding site (attribute)\|	26107004 \|Structure of musculoskeletal system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (178481025) - 19346006 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363045008 View
363045008	Connective tissue hereditary disorder (disorder)	Connective tissue hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1003407000 View
1003407000	Marfan syndrome type 1 (disorder)	Marfan syndrome type 1	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
773644000 View
773644000	Progeroid and marfanoid aspect, lipodystrophy syndrome (disorder)	Progeroid and marfanoid aspect, lipodystrophy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
763839005 View
763839005	Neonatal marfan syndrome (disorder)	Neonatal marfan syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
15993551000119100 View
15993551000119100	Disorder of eye co-occurrent and due to marfan syndrome (disorder)	Disorder of eye co-occurrent and due to marfan syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
16055631000119106 View
16055631000119106	Disorder of cardiovascular system co-occurrent and due to marfan syndrome (disorder)	Disorder of cardiovascular system co-occurrent and due to marfan syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
57201002 View
57201002	Marfanoid joint hypermobility syndrome (disorder)	Marfanoid joint hypermobility syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234035006 View
234035006	Marfan's syndrome affecting skin (disorder)	Marfan syndrome affecting skin	900000000000074008 \|Necessary but not sufficient concept 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 (0cabc68a-6f57-530a-9053-14f24a4cb56c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.4	TRUE	ALWAYS Q87.4	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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