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Terminology chevron_right Concepts chevron_right 59379005

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital pigmentary anomaly of skin (disorder)

Shortest Term

Congenital pigmentary anomaly of skin

Definition Status

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Congenital pigmentary anomaly of skin (disorder)

SCTID: 59379005, Primitive, Inactive

59379005|Congenital pigmentary anomaly of skin (disorder)|

Expression

59379005 |Congenital pigmentary anomaly of skin (disorder)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
98624012 - Congenital pigmentary anomaly of skin (en) View
98624012	en	Synonym (core metadata concept)	Congenital pigmentary anomaly of skin	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
798214015 - Congenital pigmentary anomaly of skin (disorder) (en) View
798214015	en	Fully specified name (core metadata concept)	Congenital pigmentary anomaly of skin (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
98625013 - Congenital pigmentary anomaly of skin, NOS (en) View
98625013	en	Synonym (core metadata concept)	Congenital pigmentary anomaly of skin, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (244646020) - 59379005 -> 95324001 (116680003) View
116680003 \|Is a (attribute)\|	95324001 \|Skin lesion (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (244647027) - 59379005 -> 199879009 (116680003) View
116680003 \|Is a (attribute)\|	199879009 \|Congenital anomaly of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (821460029) - 59379005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (821461025) - 59379005 -> 62307005 (116676008) View
116676008 \|Associated morphology (attribute)\|	62307005 \|Congenital pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (821462021) - 59379005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

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

Descriptions