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Terminology chevron_right Concepts chevron_right 719272007

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Component

719272007

The component that hold information about this concept.

Fully Specified Name (FSN)

Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (disorder)

Shortest Term

Progressive sensorineural deafness and hypertrophic cardiomyopathy 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

Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (disorder)

SCTID: 719272007, Primitive, Active

719272007|Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (disorder)|

en Progressive sensorineural deafness and hypertrophic cardiomyopathy syndrome
en Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome
en Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (disorder)

Expression

719272007 |Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
60700002 |Sensorineural hearing loss (disorder)| + 
232333009 |Hearing loss associated with syndrome (disorder)| + 
233873004 |Hypertrophic cardiomyopathy (disorder)| + 
363005004 |Cardiovascular system hereditary disorder (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)| = 56246009 |Hypertrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 74281007 |Myocardium structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3315791019 - Progressive sensorineural deafness and hypertrophic cardiomyopathy syndrome (en) View
3315791019	en	Synonym (core metadata concept)	Progressive sensorineural deafness and hypertrophic cardiomyopathy syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3315790018 - Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (en) View
3315790018	en	Synonym (core metadata concept)	Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3315789010 - Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (disorder) (en) View
3315789010	en	Fully specified name (core metadata concept)	Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6622893026) - 719272007 -> 362991006 (116680003) View
116680003 \|Is a (attribute)\|	362991006 \|Auditory system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16374403027) - 719272007 -> 788953003 (116680003) View
116680003 \|Is a (attribute)\|	788953003 \|Hereditary hearing loss (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6622895022) - 719272007 -> 117590005 (363698007) View
363698007 \|Finding site (attribute)\|	117590005 \|Ear structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12090993024) - 719272007 -> 91159003 (363698007) View
363698007 \|Finding site (attribute)\|	91159003 \|Structure of auditory system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6622896023) - 719272007 -> 47078008 (363714003) View
363714003 \|Interprets (attribute)\|	47078008 \|Hearing, function (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6622897025) - 719272007 -> 364644000 (363714003) View
363714003 \|Interprets (attribute)\|	364644000 \|Functional observable (observable entity)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6622889021) - 719272007 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6622890028) - 719272007 -> 60700002 (116680003) View
116680003 \|Is a (attribute)\|	60700002 \|Sensorineural hearing loss (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6622891029) - 719272007 -> 232333009 (116680003) View
116680003 \|Is a (attribute)\|	232333009 \|Hearing loss associated with syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6622892020) - 719272007 -> 233873004 (116680003) View
116680003 \|Is a (attribute)\|	233873004 \|Hypertrophic cardiomyopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6622894021) - 719272007 -> 363005004 (116680003) View
116680003 \|Is a (attribute)\|	363005004 \|Cardiovascular system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6622898024) - 719272007 -> 56246009 (116676008) View
116676008 \|Associated morphology (attribute)\|	56246009 \|Hypertrophy (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6622899027) - 719272007 -> 74281007 (363698007) View
363698007 \|Finding site (attribute)\|	74281007 \|Myocardium 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
233873004 View
233873004	Hypertrophic cardiomyopathy (disorder)	Bệnh cơ tim phì đại	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
363005004 View
363005004	Cardiovascular system hereditary disorder (disorder)	Cardiovascular system hereditary disorder	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 (67b25997-4e30-5b4c-8ef6-49ccc624e462) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	I42.2	TRUE	ALWAYS I42.2	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 (d34011cf-307f-54b4-9f3f-74de027561b5) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H90.5	TRUE	ALWAYS H90.5	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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