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Terminology chevron_right Concepts chevron_right 6874009

Production

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Component

6874009

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital keratoderma (disorder)

Shortest Term

Congenital keratoderma

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

Congenital keratoderma (disorder)

SCTID: 6874009, Defined, Active

6874009|Congenital keratoderma (disorder)|

en Congenital keratoderma
en Congenital keratoderma (disorder)

Expression

6874009 |Congenital keratoderma (disorder)|
 === 111474003 |Disorder involving the integument of fetus or newborn (disorder)| + 
707209001 |Keratoderma (disorder)| + 
66091009 |Congenital disease (disorder)| + 
816995008 |Rough skin (finding)| + 
254215005 |Erythrokeratoderma (disorder)|
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 44138005 |Keratinization, function (observable entity)| }
        { 116676008 |Associated morphology (attribute)| = 26996000 |Hyperkeratosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
12370013 - Congenital keratoderma (en) View
12370013	en	Synonym (core metadata concept)	Congenital keratoderma	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
808609014 - Congenital keratoderma (disorder) (en) View
808609014	en	Fully specified name (core metadata concept)	Congenital keratoderma (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
12371012 - Congenital keratoderma, NOS (en) View
12371012	en	Synonym (core metadata concept)	Congenital keratoderma, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15880934020) - 6874009 -> 111474003 (116680003) View
116680003 \|Is a (attribute)\|	111474003 \|Disorder involving the integument of fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12088364029) - 6874009 -> 254666005 (116680003) View
116680003 \|Is a (attribute)\|	254666005 \|Keratosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12142419020) - 6874009 -> 816995008 (116680003) View
116680003 \|Is a (attribute)\|	816995008 \|Rough skin (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1775591022) - 6874009 -> 69707008 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	69707008 \|Abnormal keratinization (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9223808025) - 6874009 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9223809022) - 6874009 -> 44138005 (363714003) View
363714003 \|Interprets (attribute)\|	44138005 \|Keratinization, function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5013312023) - 6874009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5013314024) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5032298024) - 6874009 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9064430028) - 6874009 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5981692021) - 6874009 -> 707209001 (116680003) View
116680003 \|Is a (attribute)\|	707209001 \|Keratoderma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (845578024) - 6874009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (845579027) - 6874009 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1775592026) - 6874009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3092058027) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3092059024) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5032299027) - 6874009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5032300024) - 6874009 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5032301023) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2976991022) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2976992026) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2912044029) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2912045028) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2819113022) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2819114027) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2671929026) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2671930020) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (845577025) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2512293026) - 6874009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (259926023) - 6874009 -> 95324001 (116680003) View
116680003 \|Is a (attribute)\|	95324001 \|Skin lesion (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (259925022) - 6874009 -> 254215005 (116680003) View
116680003 \|Is a (attribute)\|	254215005 \|Erythrokeratoderma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
111474003 View
111474003	Disorder involving the integument of fetus or newborn (disorder)	Perinatal dermatological disorders	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
707209001 View
707209001	Keratoderma (disorder)	Keratoderma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
816995008 View
816995008	Rough skin (finding)	Rough skin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
254215005 View
254215005	Erythrokeratoderma (disorder)	Erythrokeratoderma	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
70041004 View
70041004	Erythrokeratodermia variabilis (disorder)	Congenital poikiloderma	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722035007 View
722035007	Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder)	Mednik syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
717183001 View
717183001	Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder)	Camisa disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
239076000 View
239076000	Keratoderma with scleroatrophy of the extremities (disorder)	Huriez syndrome	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 (d86f07f9-116b-52e6-8d80-6405d7468751) 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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