dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 71619006

Production

add

Component

71619006

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital absence of ear (disorder)

Shortest Term

Congenital absence of ear

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Congenital absence of ear (disorder)

SCTID: 71619006, Defined, Active

71619006|Congenital absence of ear (disorder)|

en Congenital absence of ear
en Congenital absence of ear (disorder)

Expression

71619006 |Congenital absence of ear (disorder)|
 === 275259005 |Congenital malformation of ear (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 418560003 |Absence (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 117590005 |Ear structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
118975019 - Congenital absence of ear (en) View
118975019	en	Synonym (core metadata concept)	Congenital absence of ear	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
811805019 - Congenital absence of ear (disorder) (en) View
811805019	en	Fully specified name (core metadata concept)	Congenital absence of ear (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
118976018 - Congenital absence of ear, NOS (en) View
118976018	en	Synonym (core metadata concept)	Congenital absence of ear, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (852245025) - 71619006 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13179751029) - 71619006 -> 418560003 (116676008) View
116676008 \|Associated morphology (attribute)\|	418560003 \|Absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (852246029) - 71619006 -> 117590005 (363698007) View
363698007 \|Finding site (attribute)\|	117590005 \|Ear structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4983747022) - 71619006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4983749020) - 71619006 -> 117590005 (363698007) View
363698007 \|Finding site (attribute)\|	117590005 \|Ear structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5001289023) - 71619006 -> 702626005 (116680003) View
116680003 \|Is a (attribute)\|	702626005 \|Congenital absence (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5001290025) - 71619006 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6085267023) - 71619006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10532635024) - 71619006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (852244026) - 71619006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3400384023) - 71619006 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3400385024) - 71619006 -> 117590005 (363698007) View
363698007 \|Finding site (attribute)\|	117590005 \|Ear structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (264531029) - 71619006 -> 8380000 (116680003) View
116680003 \|Is a (attribute)\|	8380000 \|Congenital anomaly of ear (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2230777029) - 71619006 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3771776028) - 71619006 -> 275259005 (116680003) View
116680003 \|Is a (attribute)\|	275259005 \|Congenital malformation of ear (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (264532020) - 71619006 -> 204223000 (116680003) View
116680003 \|Is a (attribute)\|	204223000 \|Ear, face and neck congenital anomalies (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
275259005 View
275259005	Congenital malformation of ear (disorder)	Malformation of ear	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
71973003 View
71973003	Congenital aplasia of inner ear (disorder)	Congenital aplasia of inner ear	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
16512005 View
16512005	Congenital absence of membranous labyrinth (disorder)	Congenital absence of membranous labyrinth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
57436000 View
57436000	Congenital absence of external ear (disorder)	Anotia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
75231006 View
75231006	Congenital absence of eustachian tube (disorder)	Congenital absence of eustachian tube	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
75311005 View
75311005	Congenital absence of ossicles of ear (disorder)	Agenesis of auditory ossicles	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (70cdf6e4-667a-5a81-a488-4c25d5687039) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q16.9	TRUE	ALWAYS Q16.9	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)\|

Terminology chevron_right Concepts chevron_right 71619006

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches