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Terminology chevron_right Concepts chevron_right 722449007

Production

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Component

722449007

The component that hold information about this concept.

Fully Specified Name (FSN)

Gingival fibromatosis with progressive deafness syndrome (disorder)

Shortest Term

Jones 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

Gingival fibromatosis with progressive deafness syndrome (disorder)

SCTID: 722449007, Primitive, Active

722449007|Gingival fibromatosis with progressive deafness syndrome (disorder)|

en Gingival fibromatosis with progressive deafness syndrome
en Gingival fibromatosis with progressive deafness syndrome (disorder)
en Jones syndrome

Expression

722449007 |Gingival fibromatosis with progressive deafness syndrome (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
60700002 |Sensorineural hearing loss (disorder)| + 
109620006 |Hereditary gingival fibromatosis (disorder)| + 
232333009 |Hearing loss associated with syndrome (disorder)| + 
788953003 |Hereditary hearing loss (disorder)|
        { 363698007 |Finding site (attribute)| = 91159003 |Structure of auditory system (body structure)| }
        { 363714003 |Interprets (attribute)| = 47078008 |Hearing, function (observable entity)| }
        { 116676008 |Associated morphology (attribute)| = 19928005 |Fibromatosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 113279002 |Gingival structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3332183018 - Gingival fibromatosis with progressive deafness syndrome (en) View
3332183018	en	Synonym (core metadata concept)	Gingival fibromatosis with progressive deafness syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3332182011 - Gingival fibromatosis with progressive deafness syndrome (disorder) (en) View
3332182011	en	Fully specified name (core metadata concept)	Gingival fibromatosis with progressive deafness syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3332184012 - Jones syndrome (en) View
3332184012	en	Synonym (core metadata concept)	Jones syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6791550029) - 722449007 -> 362991006 (116680003) View
116680003 \|Is a (attribute)\|	362991006 \|Auditory system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16374437024) - 722449007 -> 788953003 (116680003) View
116680003 \|Is a (attribute)\|	788953003 \|Hereditary hearing loss (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791551025) - 722449007 -> 117590005 (363698007) View
363698007 \|Finding site (attribute)\|	117590005 \|Ear structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12091557024) - 722449007 -> 91159003 (363698007) View
363698007 \|Finding site (attribute)\|	91159003 \|Structure of auditory system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791552021) - 722449007 -> 47078008 (363714003) View
363714003 \|Interprets (attribute)\|	47078008 \|Hearing, function (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791553027) - 722449007 -> 364644000 (363714003) View
363714003 \|Interprets (attribute)\|	364644000 \|Functional observable (observable entity)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6791546020) - 722449007 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791547027) - 722449007 -> 60700002 (116680003) View
116680003 \|Is a (attribute)\|	60700002 \|Sensorineural hearing loss (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791548021) - 722449007 -> 109620006 (116680003) View
116680003 \|Is a (attribute)\|	109620006 \|Hereditary gingival fibromatosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791549029) - 722449007 -> 232333009 (116680003) View
116680003 \|Is a (attribute)\|	232333009 \|Hearing loss associated with syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791554022) - 722449007 -> 19928005 (116676008) View
116676008 \|Associated morphology (attribute)\|	19928005 \|Fibromatosis (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791555023) - 722449007 -> 113279002 (363698007) View
363698007 \|Finding site (attribute)\|	113279002 \|Gingival structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
788953003 View
788953003	Hereditary hearing loss (disorder)	Hereditary hearing loss	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
109620006 View
109620006	Hereditary gingival fibromatosis (disorder)	Hereditary gingival fibromatosis	900000000000073002 \|Sufficiently defined by necessary conditions 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
60700002 View
60700002	Sensorineural hearing loss (disorder)	Mất thính giác	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
232333009 View
232333009	Hearing loss associated with syndrome (disorder)	Syndromal deafness	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 (79c46d93-2e8b-5c18-a9e1-a729166b3427) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H90.3	TRUE	ALWAYS H90.3	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 (ca11239a-deb7-5e3a-a284-7eae317e0e88) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K06.1	TRUE	ALWAYS K06.1	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 (ed36647e-f6fc-58d5-9dfb-6b84876d3ae6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H90.3	TRUE	ALWAYS H90.3 \| 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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