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Terminology chevron_right Concepts chevron_right 897554004

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Component

897554004

The component that hold information about this concept.

Fully Specified Name (FSN)

Dermal melanocytic hamartoma (disorder)

Shortest Term

Dermal melanocytic hamartoma

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

Dermal melanocytic hamartoma (disorder)

SCTID: 897554004, Defined, Active

897554004|Dermal melanocytic hamartoma (disorder)|

en Dermal melanocytic hamartoma
en Dermal melanocytic hamartoma (disorder)

Expression

897554004 |Dermal melanocytic hamartoma (disorder)|
 === 400083002 |Congenital hamartoma of skin (disorder)| + 
49765009 |Hyperpigmentation of skin (disorder)| + 
86042009 |Congenital melanosis (disorder)| + 
205564003 |Congenital pigmentary skin anomalies (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 48010006 |Melanosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 53534000 |Dermis structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 51398009 |Hamartoma (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 53534000 |Dermis structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4034305014 - Dermal melanocytic hamartoma (en) View
4034305014	en	Synonym (core metadata concept)	Dermal melanocytic hamartoma	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4034304013 - Dermal melanocytic hamartoma (disorder) (en) View
4034304013	en	Fully specified name (core metadata concept)	Dermal melanocytic hamartoma (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13088796024) - 897554004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13110031028) - 897554004 -> 398943008 (116680003) View
116680003 \|Is a (attribute)\|	398943008 \|Congenital pigmented melanocytic nevus of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642601028) - 897554004 -> 255186004 (116680003) View
116680003 \|Is a (attribute)\|	255186004 \|Benign neoplasm of dermis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642602024) - 897554004 -> 302838006 (116680003) View
116680003 \|Is a (attribute)\|	302838006 \|Dermal cellular nevus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642604020) - 897554004 -> 112681002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112681002 \|Intradermal nevus (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15804046029) - 897554004 -> 205564003 (116680003) View
116680003 \|Is a (attribute)\|	205564003 \|Congenital pigmentary skin anomalies (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804047022) - 897554004 -> 400083002 (116680003) View
116680003 \|Is a (attribute)\|	400083002 \|Congenital hamartoma of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804048028) - 897554004 -> 49765009 (116680003) View
116680003 \|Is a (attribute)\|	49765009 \|Hyperpigmentation of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804049020) - 897554004 -> 86042009 (116680003) View
116680003 \|Is a (attribute)\|	86042009 \|Congenital melanosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804050020) - 897554004 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804051024) - 897554004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804052028) - 897554004 -> 53534000 (363698007) View
363698007 \|Finding site (attribute)\|	53534000 \|Dermis structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804053022) - 897554004 -> 51398009 (116676008) View
116676008 \|Associated morphology (attribute)\|	51398009 \|Hamartoma (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804054027) - 897554004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13088794022) - 897554004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13110032024) - 897554004 -> 400101001 (116676008) View
116676008 \|Associated morphology (attribute)\|	400101001 \|Melanocytic nevus - category (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642603025) - 897554004 -> 53534000 (363698007) View
363698007 \|Finding site (attribute)\|	53534000 \|Dermis structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13088795023) - 897554004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
49765009 View
49765009	Hyperpigmentation of skin (disorder)	Tăng sắc tố da	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
86042009 View
86042009	Congenital melanosis (disorder)	Congenital melanosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
205564003 View
205564003	Congenital pigmentary skin anomalies (disorder)	Dị tật sắc tố da bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
400083002 View
400083002	Congenital hamartoma of skin (disorder)	Congenital hamartoma of skin	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 (007818bc-b6b3-5450-b7bc-38b5b1434987) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q85.9	TRUE	ALWAYS Q85.9	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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