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Terminology chevron_right Concepts chevron_right 413835007

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Component

413835007

The component that hold information about this concept.

Fully Specified Name (FSN)

Chronic disease of immune structure (disorder)

Shortest Term

Chronic disease of immune structure

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

Chronic disease of immune structure (disorder)

SCTID: 413835007, Defined, Active

413835007|Chronic disease of immune structure (disorder)|

en Chronic disease of immune structure
en Chronic disease of immune structure (disorder)

Expression

413835007 |Chronic disease of immune structure (disorder)|
 === 27624003 |Chronic disease (disorder)| + 
414030009 |Disorder of immune structure (disorder)| : 
        { 363698007 |Finding site (attribute)| = 116003000 |Structure of immune system (body structure)| }
        { 263502005 |Clinical course (attribute)| = 90734009 |Chronic (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2534313014 - Chronic disease of immune structure (en) View
2534313014	en	Synonym (core metadata concept)	Chronic disease of immune structure	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2530849014 - Chronic disease of immune structure (disorder) (en) View
2530849014	en	Fully specified name (core metadata concept)	Chronic disease of immune structure (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2726688024) - 413835007 -> 116003000 (363698007) View
363698007 \|Finding site (attribute)\|	116003000 \|Structure of immune system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3035057026) - 413835007 -> 90734009 (263502005) View
263502005 \|Clinical course (attribute)\|	90734009 \|Chronic (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2726687025) - 413835007 -> 90734009 (260908002) View
260908002 \|Course (attribute)\|	90734009 \|Chronic (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2686460029) - 413835007 -> 27624003 (116680003) View
116680003 \|Is a (attribute)\|	27624003 \|Chronic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2686461025) - 413835007 -> 414030009 (116680003) View
116680003 \|Is a (attribute)\|	414030009 \|Disorder of immune structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
414030009 View
414030009	Disorder of immune structure (disorder)	Disorder of immune structure	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
27624003 View
27624003	Chronic disease (disorder)	Chronic disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1366434002 View
1366434002	Persistent generalized enlargement of lymph nodes (disorder)	Persistent generalised lymphadenopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
191382009 View
191382009	Chronic congestive splenomegaly (disorder)	Chronic congestive splenomegaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1220590003 View
1220590003	Familial chilblain lupus erythematosus (disorder)	Familial chilblain lupus erythematosus	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
239920006 View
239920006	Adult onset still's disease (disorder)	Wissler-fanconi syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
52636001 View
52636001	Actinic reticuloid (disorder)	Actinic reticuloid	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
829973009 View
829973009	Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis (disorder)	Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
397012002 View
397012002	Cutaneous mastocytosis (disorder)	Cutaneous mastocytosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
783787000 View
783787000	Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (disorder)	Rvcl - retinal vasculopathy cerebral leucoencephalopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
773328002 View
773328002	Infantile onset panniculitis with uveitis and systemic granulomatosis (disorder)	Infantile onset panniculitis with uveitis and systemic granulomatosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
773333003 View
773333003	Autosomal systemic lupus erythematosus (disorder)	Familial systemic lupus erythematosus	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
773662009 View
773662009	Neonatal inflammatory skin and bowel disease (disorder)	Neonatal inflammatory skin and bowel disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
773730002 View
773730002	Osteopetrosis hypogammaglobulinemia syndrome (disorder)	Autosomal recessive osteopetrosis type 7	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
768667002 View
768667002	Nucleotide binding oligomerization domain containing 2-associated autoinflammatory disease (disorder)	Yao syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
402415001 View
402415001	Schnitzler syndrome (disorder)	Schnitzler syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
16358007 View
16358007	Chronic disease of tonsils and/or adenoids (disorder)	Bệnh mạn tính của amiđan và/hoặc va	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
32035007 View
32035007	Chronic lymphadenitis (disorder)	Chronic adenitis	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 (94c52777-99e9-5138-97f3-7acb2d84fe82) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D89.9	TRUE	ALWAYS D89.9	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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