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Terminology chevron_right Concepts chevron_right 715529009

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Component

715529009

The component that hold information about this concept.

Fully Specified Name (FSN)

Progressive deafness with stapes fixation (disorder)

Shortest Term

Thies reis 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 deafness with stapes fixation (disorder)

SCTID: 715529009, Primitive, Active

715529009|Progressive deafness with stapes fixation (disorder)|

en Progressive deafness with stapes fixation
en Progressive deafness with stapes fixation (disorder)
en Stapedo-vestibular ankylosis
en Thies reis syndrome

Expression

715529009 |Progressive deafness with stapes fixation (disorder)|
 <<< 85995004 |Autosomal recessive hereditary disorder (disorder)| + 
362991006 |Auditory system hereditary disorder (disorder)| + 
54386000 |Congenital fusion of ossicles of ear (disorder)| + 
95827002 |Congenital hearing disorder (disorder)| + 
128297008 |Chronic disease of ear (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1297033003 |Abnormally fused structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 22718006 |Stapes structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        { 363714003 |Interprets (attribute)| = 47078008 |Hearing, function (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3302932016 - Progressive deafness with stapes fixation (en) View
3302932016	en	Synonym (core metadata concept)	Progressive deafness with stapes fixation	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3302931011 - Progressive deafness with stapes fixation (disorder) (en) View
3302931011	en	Fully specified name (core metadata concept)	Progressive deafness with stapes fixation (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3302933014 - Stapedo-vestibular ankylosis (en) View
3302933014	en	Synonym (core metadata concept)	Stapedo-vestibular ankylosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3302934015 - Thies Reis syndrome (en) View
3302934015	en	Synonym (core metadata concept)	Thies Reis syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (14911648026) - 715529009 -> 31883006 (116676008) View
116676008 \|Associated morphology (attribute)\|	31883006 \|Fused structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16436967027) - 715529009 -> 1297033003 (116676008) View
116676008 \|Associated morphology (attribute)\|	1297033003 \|Abnormally fused structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12251900027) - 715529009 -> 37764001 (116676008) View
116676008 \|Associated morphology (attribute)\|	37764001 \|Congenital abnormal fusion (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13069584026) - 715529009 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547045023) - 715529009 -> 91159003 (363698007) View
363698007 \|Finding site (attribute)\|	91159003 \|Structure of auditory system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12251892028) - 715529009 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12251893022) - 715529009 -> 47078008 (363714003) View
363714003 \|Interprets (attribute)\|	47078008 \|Hearing, function (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12251894027) - 715529009 -> 54386000 (116680003) View
116680003 \|Is a (attribute)\|	54386000 \|Congenital fusion of ossicles of ear (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12251895026) - 715529009 -> 95827002 (116680003) View
116680003 \|Is a (attribute)\|	95827002 \|Congenital hearing disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12251896025) - 715529009 -> 128297008 (116680003) View
116680003 \|Is a (attribute)\|	128297008 \|Chronic disease of ear (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12251897023) - 715529009 -> 22718006 (363698007) View
363698007 \|Finding site (attribute)\|	22718006 \|Stapes structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12251898029) - 715529009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12251899021) - 715529009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547043027) - 715529009 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547044022) - 715529009 -> 362991006 (116680003) View
116680003 \|Is a (attribute)\|	362991006 \|Auditory system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
95827002 View
95827002	Congenital hearing disorder (disorder)	Congenital hearing disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
54386000 View
54386000	Congenital fusion of ossicles of ear (disorder)	Congenital fusion of ear ossicles	900000000000073002 \|Sufficiently defined by necessary conditions 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
128297008 View
128297008	Chronic disease of ear (disorder)	Chronic ear disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
362991006 View
362991006	Auditory system hereditary disorder (disorder)	Auditory 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 (c93ed927-37ea-5c7d-8651-bbb0c92456a9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H74.3	TRUE	ALWAYS H74.3 \| 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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