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Terminology chevron_right Concepts chevron_right 771184001

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Component

771184001

The component that hold information about this concept.

Fully Specified Name (FSN)

Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder)

Shortest Term

Leucoencephalopathy, palmoplantar keratoderma syndrome

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

Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder)

SCTID: 771184001, Primitive, Active

771184001|Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder)|

en Leucoencephalopathy, palmoplantar keratoderma syndrome
en Leukoencephalopathy, palmoplantar keratoderma syndrome
en Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder)

Expression

771184001 |Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder)|
 <<< 22811006 |Leukoencephalopathy (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
402773000 |Punctate palmoplantar keratoderma (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
254214009 |Inherited disorder of keratinization (disorder)| + 
829993001 |Rough skin of hands (finding)| : 
        { 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)| = 68523003 |Cerebral white matter structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 26996000 |Hyperkeratosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 37136002 |Skin structure of sole of foot (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 26996000 |Hyperkeratosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 70887009 |Skin structure of palmar area of hand (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3789564010 - Leucoencephalopathy, palmoplantar keratoderma syndrome (en) View
3789564010	en	Synonym (core metadata concept)	Leucoencephalopathy, palmoplantar keratoderma syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3704804017 - Leukoencephalopathy, palmoplantar keratoderma syndrome (en) View
3704804017	en	Synonym (core metadata concept)	Leukoencephalopathy, palmoplantar keratoderma syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3704805016 - Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder) (en) View
3704805016	en	Fully specified name (core metadata concept)	Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12094951029) - 771184001 -> 254666005 (116680003) View
116680003 \|Is a (attribute)\|	254666005 \|Keratosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12142428021) - 771184001 -> 816995008 (116680003) View
116680003 \|Is a (attribute)\|	816995008 \|Rough skin (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12247538023) - 771184001 -> 829993001 (116680003) View
116680003 \|Is a (attribute)\|	829993001 \|Rough skin of hands (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9662659025) - 771184001 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12094947026) - 771184001 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094948020) - 771184001 -> 70887009 (363698007) View
363698007 \|Finding site (attribute)\|	70887009 \|Skin structure of palmar area of hand (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094949028) - 771184001 -> 254214009 (116680003) View
116680003 \|Is a (attribute)\|	254214009 \|Inherited disorder of keratinization (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12094950028) - 771184001 -> 37136002 (363698007) View
363698007 \|Finding site (attribute)\|	37136002 \|Skin structure of sole of foot (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648754025) - 771184001 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9651270026) - 771184001 -> 41847000 (246454002) View
246454002 \|Occurrence (attribute)\|	41847000 \|Adulthood (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9662657028) - 771184001 -> 713152004 (246454002) View
246454002 \|Occurrence (attribute)\|	713152004 \|Early childhood (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11265573025) - 771184001 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648745028) - 771184001 -> 22811006 (116680003) View
116680003 \|Is a (attribute)\|	22811006 \|Leukoencephalopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648749023) - 771184001 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648750023) - 771184001 -> 402773000 (116680003) View
116680003 \|Is a (attribute)\|	402773000 \|Punctate palmoplantar keratoderma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648751022) - 771184001 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648752026) - 771184001 -> 44138005 (363714003) View
363714003 \|Interprets (attribute)\|	44138005 \|Keratinization, function (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9648753020) - 771184001 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9651271027) - 771184001 -> 68523003 (363698007) View
363698007 \|Finding site (attribute)\|	68523003 \|Cerebral white matter structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9662658022) - 771184001 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
829993001 View
829993001	Rough skin of hands (finding)	Rough skin of hands	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
254214009 View
254214009	Inherited disorder of keratinization (disorder)	Inherited disorder of keratinisation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
22811006 View
22811006	Leukoencephalopathy (disorder)	Leucoencephalopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
402773000 View
402773000	Punctate palmoplantar keratoderma (disorder)	Punctate palmoplantar keratoderma	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363235000 View
363235000	Hereditary disorder of nervous system (disorder)	Hereditary disorder of nervous system	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 (016f301a-f0d3-5d18-aeae-27cbb0536c26) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G93.4	TRUE	ALWAYS G93.4	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)\|
ExtendedMap object (0f9a2386-259a-57a7-a54b-f7a20947812b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q82.8	TRUE	ALWAYS Q82.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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 (2addb16b-616a-5862-ba2f-8fde314560b6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G93.4	TRUE	ALWAYS G93.4	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)\|
ExtendedMap object (974babe6-9c1e-574b-a519-80cd4677eff7) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q82.8	TRUE	ALWAYS Q82.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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