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Terminology chevron_right Concepts chevron_right 315058005

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Component

315058005

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary nonpolyposis colon cancer (disorder)

Shortest Term

Lynch 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

Hereditary nonpolyposis colon cancer (disorder)

SCTID: 315058005, Primitive, Active

315058005|Hereditary nonpolyposis colon cancer (disorder)|

vi Hnpcc - ung thư đại tràng không phát sinh polyp di truyền
en Hereditary nonpolyposis colon cancer
en Hereditary nonpolyposis colon cancer (disorder)
en Hnpcc - hereditary nonpolyposis colorectal cancer
en Hnpcc - hereditary nonpolyposis colon cancer

Expression

315058005 |Hereditary nonpolyposis colon cancer (disorder)|
 <<< 93761005 |Primary malignant neoplasm of colon (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
699346009 |Hereditary cancer-predisposing syndrome (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1240414004 |Malignant neoplasm (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 71854001 |Colon structure (body structure)|,
370135005 |Pathological process (attribute)| = 1234914003 |Malignant proliferation of primary neoplasm (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
582791000003111 - HNPCC - ung thư đại tràng không phát sinh polyp di truyền (vi) View
582791000003111	vi	Synonym (core metadata concept)	HNPCC - ung thư đại tràng không phát sinh polyp di truyền	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
459527013 - Hereditary nonpolyposis colon cancer (en) View
459527013	en	Synonym (core metadata concept)	Hereditary nonpolyposis colon cancer	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
711910018 - Hereditary nonpolyposis colon cancer (disorder) (en) View
711910018	en	Fully specified name (core metadata concept)	Hereditary nonpolyposis colon cancer (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2971579012 - Lynch syndrome (en) View
2971579012	en	Synonym (core metadata concept)	Lynch syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
2971230015 - HNPCC - hereditary nonpolyposis colorectal cancer (en) View
2971230015	en	Synonym (core metadata concept)	HNPCC - hereditary nonpolyposis colorectal cancer	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
459528015 - HNPCC - hereditary nonpolyposis colon cancer (en) View
459528015	en	Synonym (core metadata concept)	HNPCC - hereditary nonpolyposis colon cancer	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4636996025) - 315058005 -> 86049000 (116676008) View
116676008 \|Associated morphology (attribute)\|	86049000 \|Malignant neoplasm, primary (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4636997023) - 315058005 -> 71854001 (363698007) View
363698007 \|Finding site (attribute)\|	71854001 \|Colon structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15420477029) - 315058005 -> 71854001 (363698007) View
363698007 \|Finding site (attribute)\|	71854001 \|Colon structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15420478023) - 315058005 -> 1240414004 (116676008) View
116676008 \|Associated morphology (attribute)\|	1240414004 \|Malignant neoplasm (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15420479026) - 315058005 -> 1234914003 (370135005) View
370135005 \|Pathological process (attribute)\|	1234914003 \|Malignant proliferation of primary neoplasm (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6611730023) - 315058005 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4799048026) - 315058005 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4799049023) - 315058005 -> 699346009 (116680003) View
116680003 \|Is a (attribute)\|	699346009 \|Hereditary cancer-predisposing syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3331645025) - 315058005 -> 14742008 (363698007) View
363698007 \|Finding site (attribute)\|	14742008 \|Large intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3331646029) - 315058005 -> 86049000 (116676008) View
116676008 \|Associated morphology (attribute)\|	86049000 \|Malignant neoplasm, primary (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3331647022) - 315058005 -> 71854001 (363698007) View
363698007 \|Finding site (attribute)\|	71854001 \|Colon structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3331648028) - 315058005 -> 367651003 (116676008) View
116676008 \|Associated morphology (attribute)\|	367651003 \|Malignant neoplasm of primary, secondary, or uncertain origin (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (679556027) - 315058005 -> 86049000 (116676008) View
116676008 \|Associated morphology (attribute)\|	86049000 \|Malignant neoplasm, primary (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (679557020) - 315058005 -> 71854001 (363698007) View
363698007 \|Finding site (attribute)\|	71854001 \|Colon structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (679558026) - 315058005 -> 367651003 (116676008) View
116676008 \|Associated morphology (attribute)\|	367651003 \|Malignant neoplasm of primary, secondary, or uncertain origin (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1752710028) - 315058005 -> 14742008 (363698007) View
363698007 \|Finding site (attribute)\|	14742008 \|Large intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (679555028) - 315058005 -> 367636007 (308489006) View
308489006 \|Pathological process (qualifier value)\|	367636007 \|Malignant neoplastic process (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (142568021) - 315058005 -> 93761005 (116680003) View
116680003 \|Is a (attribute)\|	93761005 \|Primary malignant neoplasm of colon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
699346009 View
699346009	Hereditary cancer-predisposing syndrome (disorder)	Hereditary neoplastic syndrome	900000000000074008 \|Necessary but not sufficient concept 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
93761005 View
93761005	Primary malignant neoplasm of colon (disorder)	Malignant neoplasm of colon	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1197359006 View
1197359006	Familial colorectal cancer type x (disorder)	Familial colorectal cancer type x	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 (1fb7ea63-c0e8-5609-863c-b4e6b8a6f4e8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	C18.9	TRUE	ALWAYS C18.9 \| POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE	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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