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Terminology chevron_right Concepts chevron_right 186118006

Production

add

Component

186118006

The component that hold information about this concept.

Fully Specified Name (FSN)

Addison melanoderma (disorder)

Shortest Term

Asthenia pigmentosa

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

Addison melanoderma (disorder)

SCTID: 186118006, Defined, Active

186118006|Addison melanoderma (disorder)|

en Asthenia pigmentosa
en Addison melanoderma (disorder)
en Addison melanoderma

Expression

186118006 |Addison melanoderma (disorder)|
 === 49238001 |Melanoderma (disorder)| + 
402611000 |Hypermelanosis due to endocrine disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 48010006 |Melanosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)|,
246454002 |Occurrence (attribute)| = 767023003 |Period of life beginning after birth and ending before death (qualifier value)| }
        { 42752001 |Due to (attribute)| = 363732003 |Addison's disease (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
286110019 - Asthenia pigmentosa (en) View
286110019	en	Synonym (core metadata concept)	Asthenia pigmentosa	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
569099016 - Addison melanoderma (disorder) (en) View
569099016	en	Fully specified name (core metadata concept)	Addison melanoderma (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
286109012 - Addison melanoderma (en) View
286109012	en	Synonym (core metadata concept)	Addison melanoderma	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12209801024) - 186118006 -> 402611000 (116680003) View
116680003 \|Is a (attribute)\|	402611000 \|Hypermelanosis due to endocrine disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2777740024) - 186118006 -> 363732003 (42752001) View
42752001 \|Due to (attribute)\|	363732003 \|Addison's disease (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2708576029) - 186118006 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3354949029) - 186118006 -> 4830009 (116676008) View
116676008 \|Associated morphology (attribute)\|	4830009 \|Hyperpigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9335398024) - 186118006 -> 767023003 (246454002) View
246454002 \|Occurrence (attribute)\|	767023003 \|Period of life beginning after birth and ending before death (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9335399027) - 186118006 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (459104021) - 186118006 -> 4830009 (116676008) View
116676008 \|Associated morphology (attribute)\|	4830009 \|Hyperpigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2777741023) - 186118006 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3354950029) - 186118006 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (459106023) - 186118006 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (459105022) - 186118006 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (17814020) - 186118006 -> 49238001 (116680003) View
116680003 \|Is a (attribute)\|	49238001 \|Melanoderma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
402611000 View
402611000	Hypermelanosis due to endocrine disorder (disorder)	Hypermelanosis due to endocrine disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
49238001 View
49238001	Melanoderma (disorder)	Melanoderma	900000000000074008 \|Necessary but not sufficient concept 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 (96ac1534-97de-5478-80c0-ae275d0e0cbb) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L81.4	TRUE	ALWAYS L81.4	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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