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Terminology chevron_right Concepts chevron_right 726019003

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Component

726019003

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial malignant melanoma of skin (disorder)

Shortest Term

Familial malignant melanoma of skin

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

Familial malignant melanoma of skin (disorder)

SCTID: 726019003, Defined, Active

726019003|Familial malignant melanoma of skin (disorder)|

en Familial cutaneous malignant melanoma
en Familial malignant melanoma of skin
en Familial malignant melanoma of skin (disorder)

Expression

726019003 |Familial malignant melanoma of skin (disorder)|
 === 55352002 |Familial neoplastic disease (disorder)| + 
93655004 |Malignant melanoma of skin (disorder)| + 
363185004 |Hereditary disorder of the integument (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1162635006 |Malignant melanoma (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
3447505011 - Familial cutaneous malignant melanoma (en) View
3447505011	en	Synonym (core metadata concept)	Familial cutaneous malignant melanoma	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3447504010 - Familial malignant melanoma of skin (en) View
3447504010	en	Synonym (core metadata concept)	Familial malignant melanoma of skin	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3447503016 - Familial malignant melanoma of skin (disorder) (en) View
3447503016	en	Fully specified name (core metadata concept)	Familial malignant melanoma of skin (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6913264029) - 726019003 -> 372156000 (116676008) View
116676008 \|Associated morphology (attribute)\|	372156000 \|Malignant melanoma - category (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13890743022) - 726019003 -> 1162635006 (116676008) View
116676008 \|Associated morphology (attribute)\|	1162635006 \|Malignant melanoma (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913261021) - 726019003 -> 55352002 (116680003) View
116680003 \|Is a (attribute)\|	55352002 \|Familial neoplastic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913262025) - 726019003 -> 93655004 (116680003) View
116680003 \|Is a (attribute)\|	93655004 \|Malignant melanoma of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913263024) - 726019003 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6913265028) - 726019003 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
55352002 View
55352002	Familial neoplastic disease (disorder)	Familial neoplastic disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93655004 View
93655004	Malignant melanoma of skin (disorder)	Ung thư da	900000000000073002 \|Sufficiently defined by necessary conditions 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 (84537bd5-58a4-560d-baa6-32a4df315701) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z80.8	TRUE	ALWAYS Z80.8	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)\|
ExtendedMap object (d6073b78-7e6b-5cd1-9ccc-7476aba767ca) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	C43.9	TRUE	ALWAYS C43.9 \| 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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