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Terminology chevron_right Concepts chevron_right 239085000

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Component

239085000

The component that hold information about this concept.

Fully Specified Name (FSN)

Symmetrical dyschromatosis of extremities (disorder)

Shortest Term

Acropigmentation of dohi

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

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

Summary

Symmetrical dyschromatosis of extremities (disorder)

SCTID: 239085000, Primitive, Active

239085000|Symmetrical dyschromatosis of extremities (disorder)|

en Symmetrical dyschromatosis of extremities
en Symmetrical dyschromatosis of extremities (disorder)
en Acropigmentation of dohi
en Reticulate acropigmentation of dohi

Expression

239085000 |Symmetrical dyschromatosis of extremities (disorder)|
 <<< 239079007 |Inherited cutaneous hyperpigmentation (disorder)| + 
60475009 |Congenital anomaly of limb (disorder)| + 
280134004 |Disorder of soft tissue of limb (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4830009 |Hyperpigmentation (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 116370005 |Skin structure of extremity (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
358299011 - Symmetrical dyschromatosis of extremities (en) View
358299011	en	Synonym (core metadata concept)	Symmetrical dyschromatosis of extremities	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
628054017 - Symmetrical dyschromatosis of extremities (disorder) (en) View
628054017	en	Fully specified name (core metadata concept)	Symmetrical dyschromatosis of extremities (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
358300015 - Acropigmentation of Dohi (en) View
358300015	en	Synonym (core metadata concept)	Acropigmentation of Dohi	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
358301016 - Reticulate acropigmentation of Dohi (en) View
358301016	en	Synonym (core metadata concept)	Reticulate acropigmentation of Dohi	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16362764024) - 239085000 -> 280134004 (116680003) View
116680003 \|Is a (attribute)\|	280134004 \|Disorder of soft tissue of limb (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2765478020) - 239085000 -> 128605003 (116680003) View
116680003 \|Is a (attribute)\|	128605003 \|Disorder of extremity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5031769022) - 239085000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5031770023) - 239085000 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5031771022) - 239085000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10532100023) - 239085000 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532101022) - 239085000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532102026) - 239085000 -> 60475009 (116680003) View
116680003 \|Is a (attribute)\|	60475009 \|Congenital anomaly of limb (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (530652024) - 239085000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3327070028) - 239085000 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3327071029) - 239085000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (461658029) - 239085000 -> 4830009 (116676008) View
116676008 \|Associated morphology (attribute)\|	4830009 \|Hyperpigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1730805021) - 239085000 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2575500028) - 239085000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2779441028) - 239085000 -> 116370005 (363698007) View
363698007 \|Finding site (attribute)\|	116370005 \|Skin structure of extremity (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3327072020) - 239085000 -> 116370005 (363698007) View
363698007 \|Finding site (attribute)\|	116370005 \|Skin structure of extremity (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3440217024) - 239085000 -> 4830009 (116676008) View
116676008 \|Associated morphology (attribute)\|	4830009 \|Hyperpigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (530655021) - 239085000 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (461659021) - 239085000 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (55195021) - 239085000 -> 239079007 (116680003) View
116680003 \|Is a (attribute)\|	239079007 \|Inherited cutaneous hyperpigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
239079007 View
239079007	Inherited cutaneous hyperpigmentation (disorder)	Inherited cutaneous hyperpigmentation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
280134004 View
280134004	Disorder of soft tissue of limb (disorder)	Disorder of soft tissue of limb	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
60475009 View
60475009	Congenital anomaly of limb (disorder)	Congenital anomaly of limb	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 (cc7d3514-2758-589f-bcd3-720a2038e911) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L81.9	TRUE	ALWAYS L81.9	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)\|
ExtendedMap object (e553c8ef-8241-52fc-ab8d-19214a77784b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L81.8	TRUE	ALWAYS L81.8	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)\|

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