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Terminology chevron_right Concepts chevron_right 787410005

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Component

787410005

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary mixed polyposis syndrome (disorder)

Shortest Term

Hereditary mixed polyposis 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 mixed polyposis syndrome (disorder)

SCTID: 787410005, Primitive, Active

787410005|Hereditary mixed polyposis syndrome (disorder)|

en Hereditary mixed polyposis syndrome
en Hereditary mixed polyposis syndrome (disorder)
en Hmps - hereditary mixed polyposis syndrome

Expression

787410005 |Hereditary mixed polyposis syndrome (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
254589009 |Intestinal polyposis syndrome (disorder)| + 
699346009 |Hereditary cancer-predisposing syndrome (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 41329004 |Polyp (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 113276009 |Intestinal structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3775329015 - Hereditary mixed polyposis syndrome (en) View
3775329015	en	Synonym (core metadata concept)	Hereditary mixed polyposis syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3775330013 - Hereditary mixed polyposis syndrome (disorder) (en) View
3775330013	en	Fully specified name (core metadata concept)	Hereditary mixed polyposis syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3775332017 - HMPS - hereditary mixed polyposis syndrome (en) View
3775332017	en	Synonym (core metadata concept)	HMPS - hereditary mixed polyposis syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11544564028) - 787410005 -> 113276009 (363698007) View
363698007 \|Finding site (attribute)\|	113276009 \|Intestinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544565027) - 787410005 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544566026) - 787410005 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544567024) - 787410005 -> 254589009 (116680003) View
116680003 \|Is a (attribute)\|	254589009 \|Intestinal polyposis syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544568025) - 787410005 -> 41329004 (116676008) View
116676008 \|Associated morphology (attribute)\|	41329004 \|Polyp (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544569022) - 787410005 -> 699346009 (116680003) View
116680003 \|Is a (attribute)\|	699346009 \|Hereditary cancer-predisposing syndrome (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
254589009 View
254589009	Intestinal polyposis syndrome (disorder)	Intestinal polyposis syndrome	900000000000074008 \|Necessary but not sufficient concept 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

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (9cf91a9a-38a3-57d6-b73b-63122a8655c4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D12.6	TRUE	ALWAYS D12.6 \| 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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