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Terminology chevron_right Concepts chevron_right 190590004

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Progeria (disorder)

Shortest Term

Progeria

Definition Status

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

Summary

Progeria (disorder)

SCTID: 190590004, Primitive, Inactive

190590004|Progeria (disorder)|

Expression

190590004 |Progeria (disorder)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
292945011 - Adult premature ageing syndrome (en) View
292945011	en	Synonym (core metadata concept)	Adult premature ageing syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
292947015 - Adult premature aging syndrome (en) View
292947015	en	Synonym (core metadata concept)	Adult premature aging syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
292944010 - Premature ageing syndrome (en) View
292944010	en	Synonym (core metadata concept)	Premature ageing syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
292948013 - Premature aging syndrome (en) View
292948013	en	Synonym (core metadata concept)	Premature aging syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
292949017 - Progeria (en) View
292949017	en	Synonym (core metadata concept)	Progeria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
574189012 - Progeria (disorder) (en) View
574189012	en	Fully specified name (core metadata concept)	Progeria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
292946012 - Progeria syndrome (en) View
292946012	en	Synonym (core metadata concept)	Progeria syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (19181026) - 190590004 -> 86095007 (116680003) View
116680003 \|Is a (attribute)\|	86095007 \|Inborn error of metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (19182022) - 190590004 -> 38164009 (116680003) View
116680003 \|Is a (attribute)\|	38164009 \|Congenital anomaly of integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (19183028) - 190590004 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (462317029) - 190590004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (462318023) - 190590004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1651892028) - 190590004 -> 95320005 (116680003) View
116680003 \|Is a (attribute)\|	95320005 \|Disorder of skin (disorder)\|	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

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (19181026) - 190590004 -> 86095007 (116680003) View
116680003 \|Is a (attribute)\|	86095007 \|Inborn error of metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (19182022) - 190590004 -> 38164009 (116680003) View
116680003 \|Is a (attribute)\|	38164009 \|Congenital anomaly of integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (19183028) - 190590004 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (462317029) - 190590004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (462318023) - 190590004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1651892028) - 190590004 -> 95320005 (116680003) View
116680003 \|Is a (attribute)\|	95320005 \|Disorder of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Descriptions