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Terminology chevron_right Concepts chevron_right 1162799008

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Component

1162799008

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary leiomyomatosis and renal cell carcinoma (disorder)

Shortest Term

Familial leiomyomatosis with renal carcinoma

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 leiomyomatosis and renal cell carcinoma (disorder)

SCTID: 1162799008, Primitive, Active

1162799008|Hereditary leiomyomatosis and renal cell carcinoma (disorder)|

en Familial leiomyomatosis and renal cell cancer
en Familial leiomyomatosis with renal carcinoma
en Hereditary leiomyomatosis and renal cell cancer
en Hereditary leiomyomatosis and renal cell carcinoma
en Hereditary leiomyomatosis and renal cell carcinoma (disorder)
en Hereditary leiomyomatosis with renal carcinoma
en Hlrcc - hereditary leiomyomatosis and renal cell cancer

Expression

1162799008 |Hereditary leiomyomatosis and renal cell carcinoma (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
363185004 |Hereditary disorder of the integument (disorder)| + 
699346009 |Hereditary cancer-predisposing syndrome (disorder)| + 
254767008 |Cutaneous leiomyoma (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1162890002 |Leiomyoma (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4591496014 - Familial leiomyomatosis and renal cell cancer (en) View
4591496014	en	Synonym (core metadata concept)	Familial leiomyomatosis and renal cell cancer	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4591492011 - Familial leiomyomatosis with renal carcinoma (en) View
4591492011	en	Synonym (core metadata concept)	Familial leiomyomatosis with renal carcinoma	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4591505018 - Hereditary leiomyomatosis and renal cell cancer (en) View
4591505018	en	Synonym (core metadata concept)	Hereditary leiomyomatosis and renal cell cancer	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4591504019 - Hereditary leiomyomatosis and renal cell carcinoma (en) View
4591504019	en	Synonym (core metadata concept)	Hereditary leiomyomatosis and renal cell carcinoma	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4591503013 - Hereditary leiomyomatosis and renal cell carcinoma (disorder) (en) View
4591503013	en	Fully specified name (core metadata concept)	Hereditary leiomyomatosis and renal cell carcinoma (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4591493018 - Hereditary leiomyomatosis with renal carcinoma (en) View
4591493018	en	Synonym (core metadata concept)	Hereditary leiomyomatosis with renal carcinoma	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4591491016 - HLRCC - hereditary leiomyomatosis and renal cell cancer (en) View
4591491016	en	Synonym (core metadata concept)	HLRCC - hereditary leiomyomatosis and renal cell cancer	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13895840026) - 1162799008 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13895842023) - 1162799008 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13895843029) - 1162799008 -> 699346009 (116680003) View
116680003 \|Is a (attribute)\|	699346009 \|Hereditary cancer-predisposing syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13895845020) - 1162799008 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13897718025) - 1162799008 -> 254767008 (116680003) View
116680003 \|Is a (attribute)\|	254767008 \|Cutaneous leiomyoma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13897719022) - 1162799008 -> 1162890002 (116676008) View
116676008 \|Associated morphology (attribute)\|	1162890002 \|Leiomyoma (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
254767008 View
254767008	Cutaneous leiomyoma (disorder)	Piloleiomyoma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
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
363185004 View
363185004	Hereditary disorder of the integument (disorder)	Hereditary disorder of the integument	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 (5b61d113-d9ed-51ef-aaa2-68baa474c669) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D21.9	TRUE	ALWAYS D21.9 \| 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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