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Terminology chevron_right Concepts chevron_right 254215005

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Component

254215005

The component that hold information about this concept.

Fully Specified Name (FSN)

Erythrokeratoderma (disorder)

Shortest Term

Erythrokeratoderma

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

Erythrokeratoderma (disorder)

SCTID: 254215005, Primitive, Active

254215005|Erythrokeratoderma (disorder)|

en Erythrokeratoderma
en Erythrokeratoderma (disorder)

Expression

254215005 |Erythrokeratoderma (disorder)|
 <<< 254214009 |Inherited disorder of keratinization (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 44138005 |Keratinization, function (observable entity)| }
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 48075008 |Structure of integumentary system (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
378441011 - Erythrokeratoderma (en) View
378441011	en	Synonym (core metadata concept)	Erythrokeratoderma	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
645076019 - Erythrokeratoderma (disorder) (en) View
645076019	en	Fully specified name (core metadata concept)	Erythrokeratoderma (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9064458020) - 254215005 -> 48075008 (363698007) View
363698007 \|Finding site (attribute)\|	48075008 \|Structure of integumentary system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11265473028) - 254215005 -> 48075008 (363698007) View
363698007 \|Finding site (attribute)\|	48075008 \|Structure of integumentary system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11265474023) - 254215005 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1736468023) - 254215005 -> 69707008 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	69707008 \|Abnormal keratinization (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9181641025) - 254215005 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9181642021) - 254215005 -> 44138005 (363714003) View
363714003 \|Interprets (attribute)\|	44138005 \|Keratinization, function (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5032103027) - 254215005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5032104022) - 254215005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5032105023) - 254215005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (580132020) - 254215005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3290563027) - 254215005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3290564022) - 254215005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (580131029) - 254215005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1736467029) - 254215005 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (74334020) - 254215005 -> 254214009 (116680003) View
116680003 \|Is a (attribute)\|	254214009 \|Inherited disorder of keratinization (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
254214009 View
254214009	Inherited disorder of keratinization (disorder)	Inherited disorder of keratinisation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1179293006 View
1179293006	Erythrokeratodermia cardiomyopathy syndrome (disorder)	Erythrokeratodermia cardiomyopathy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
783555001 View
783555001	Hypotrichosis and deafness syndrome (disorder)	Hypotrichosis and deafness syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
719255000 View
719255000	Spinocerebellar ataxia type 34 (disorder)	Spinocerebellar ataxia type 34	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
6874009 View
6874009	Congenital keratoderma (disorder)	Congenital keratoderma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
239062001 View
239062001	Erythrokeratoderma en cocardes (disorder)	Maladie de degos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
24559001 View
24559001	Mutilating keratoderma (disorder)	Vohwinkel syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
239063006 View
239063006	Erythrokeratoderma progressiva of gottron (disorder)	Erythrokeratoderma progressiva of gottron	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
268282005 View
268282005	Ichthyosiform erythroderma (disorder)	Ichthyosiform dermatosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (2440e134-9ee4-5cc9-ba10-098da0ebbd60) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q82.8	TRUE	ALWAYS Q82.8	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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