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Terminology chevron_right Concepts chevron_right 765096001

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Component

765096001

The component that hold information about this concept.

Fully Specified Name (FSN)

Punctate palmoplantar keratoderma type 2 (disorder)

Shortest Term

Punctate palmoplantar keratoderma type 2

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

Punctate palmoplantar keratoderma type 2 (disorder)

SCTID: 765096001, Primitive, Active

765096001|Punctate palmoplantar keratoderma type 2 (disorder)|

en Punctate palmoplantar keratoderma type 2
en Punctate palmoplantar keratoderma type 2 (disorder)

Expression

765096001 |Punctate palmoplantar keratoderma type 2 (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
402773000 |Punctate palmoplantar keratoderma (disorder)| : 
        { 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
3656394014 - Punctate palmoplantar keratoderma type 2 (en) View
3656394014	en	Synonym (core metadata concept)	Punctate palmoplantar keratoderma type 2	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3656393015 - Punctate palmoplantar keratoderma type 2 (disorder) (en) View
3656393015	en	Fully specified name (core metadata concept)	Punctate palmoplantar keratoderma type 2 (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9214496022) - 765096001 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9214497029) - 765096001 -> 44138005 (363714003) View
363714003 \|Interprets (attribute)\|	44138005 \|Keratinization, function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9224824021) - 765096001 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12095174021) - 765096001 -> 37136002 (363698007) View
363698007 \|Finding site (attribute)\|	37136002 \|Skin structure of sole of foot (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12095175022) - 765096001 -> 70887009 (363698007) View
363698007 \|Finding site (attribute)\|	70887009 \|Skin structure of palmar area of hand (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12095176023) - 765096001 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9214494020) - 765096001 -> 363185004 (116680003) View
116680003 \|Is a (attribute)\|	363185004 \|Hereditary disorder of the integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9214493025) - 765096001 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9214495021) - 765096001 -> 402773000 (116680003) View
116680003 \|Is a (attribute)\|	402773000 \|Punctate palmoplantar keratoderma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9224823026) - 765096001 -> 26996000 (116676008) View
116676008 \|Associated morphology (attribute)\|	26996000 \|Hyperkeratosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
402773000 View
402773000	Punctate palmoplantar keratoderma (disorder)	Punctate palmoplantar keratoderma	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept 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 (387e48b1-a16b-59e3-8854-e4c0d93ad3bc) 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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