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Terminology chevron_right Concepts chevron_right 11131009

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Component

11131009

The component that hold information about this concept.

Fully Specified Name (FSN)

Malignant atrophic papulosis (disorder)

Shortest Term

Degos' disease

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

Malignant atrophic papulosis (disorder)

SCTID: 11131009, Primitive, Inactive

11131009|Malignant atrophic papulosis (disorder)|

en Erythrokeratoderma en cocardes
en Lethal cutaneous and gastrointestinal arteriolar thrombosis
en Malignant atrophic papulosis
en Malignant atrophic papulosis (disorder)
en Degos' disease
en Maladie de degos
en Malignant atrophic papulosis of degos

Expression

11131009 |Malignant atrophic papulosis (disorder)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
360932012 - Erythrokeratoderma en cocardes (en) View
360932012	en	Synonym (core metadata concept)	Erythrokeratoderma en cocardes	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
360934013 - Lethal cutaneous and gastrointestinal arteriolar thrombosis (en) View
360934013	en	Synonym (core metadata concept)	Lethal cutaneous and gastrointestinal arteriolar thrombosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
19288016 - Malignant atrophic papulosis (en) View
19288016	en	Synonym (core metadata concept)	Malignant atrophic papulosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
630199018 - Malignant atrophic papulosis (disorder) (en) View
630199018	en	Fully specified name (core metadata concept)	Malignant atrophic papulosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
19289012 - Degos' disease (en) View
19289012	en	Synonym (core metadata concept)	Degos' disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
360931017 - Maladie de Degos (en) View
360931017	en	Synonym (core metadata concept)	Maladie de Degos	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
360933019 - Malignant atrophic papulosis of Degos (en) View
360933019	en	Synonym (core metadata concept)	Malignant atrophic papulosis of Degos	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (58281025) - 11131009 -> 11263005 (116680003) View
116680003 \|Is a (attribute)\|	11263005 \|Vascular disease of the skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (58282021) - 11131009 -> 70041004 (116680003) View
116680003 \|Is a (attribute)\|	70041004 \|Erythrokeratodermia variabilis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538979021) - 11131009 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538980024) - 11131009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538982027) - 11131009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538983021) - 11131009 -> 59820001 (363698007) View
363698007 \|Finding site (attribute)\|	59820001 \|Blood vessel structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538984026) - 11131009 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1658125026) - 11131009 -> 362975008 (116680003) View
116680003 \|Is a (attribute)\|	362975008 \|Degenerative disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1732181024) - 11131009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1732182028) - 11131009 -> 69707008 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	69707008 \|Abnormal keratinization (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1732183022) - 11131009 -> 51833009 (363698007) View
363698007 \|Finding site (attribute)\|	51833009 \|Peripheral blood vessel structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2200764021) - 11131009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1708160027) - 11131009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538981023) - 11131009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	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 (58281025) - 11131009 -> 11263005 (116680003) View
116680003 \|Is a (attribute)\|	11263005 \|Vascular disease of the skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (58282021) - 11131009 -> 70041004 (116680003) View
116680003 \|Is a (attribute)\|	70041004 \|Erythrokeratodermia variabilis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538979021) - 11131009 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538980024) - 11131009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538982027) - 11131009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538983021) - 11131009 -> 59820001 (363698007) View
363698007 \|Finding site (attribute)\|	59820001 \|Blood vessel structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538984026) - 11131009 -> 13331008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13331008 \|Atrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1658125026) - 11131009 -> 362975008 (116680003) View
116680003 \|Is a (attribute)\|	362975008 \|Degenerative disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1732181024) - 11131009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1732182028) - 11131009 -> 69707008 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	69707008 \|Abnormal keratinization (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1732183022) - 11131009 -> 51833009 (363698007) View
363698007 \|Finding site (attribute)\|	51833009 \|Peripheral blood vessel structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2200764021) - 11131009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1708160027) - 11131009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (538981023) - 11131009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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