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Terminology chevron_right Concepts chevron_right 1237343009

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Component

1237343009

The component that hold information about this concept.

Fully Specified Name (FSN)

Otodental syndrome (disorder)

Shortest Term

Otodental 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

Otodental syndrome (disorder)

SCTID: 1237343009, Primitive, Active

1237343009|Otodental syndrome (disorder)|

en Otodental dysplasia
en Otodental syndrome
en Otodental syndrome (disorder)

Expression

1237343009 |Otodental syndrome (disorder)|
 <<< 103276001 |Decreased hearing (finding)| + 
1083811000119108 |High frequency sensorineural hearing loss of bilateral ears (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
1148766007 |Hereditary disorder of tooth (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
707310009 |Globodontia (disorder)| + 
788953003 |Hereditary hearing loss (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 442021009 |Enlargement (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 38199008 |Tooth structure (body structure)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 1250004 |Decreased (qualifier value)|,
363714003 |Interprets (attribute)| = 47078008 |Hearing, function (observable entity)| }
        { 363698007 |Finding site (attribute)| = 73401004 |Left inner ear structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 76473007 |Right inner ear structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5097802016 - Otodental dysplasia (en) View
5097802016	en	Synonym (core metadata concept)	Otodental dysplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
5097803014 - Otodental syndrome (en) View
5097803014	en	Synonym (core metadata concept)	Otodental syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5097801011 - Otodental syndrome (disorder) (en) View
5097801011	en	Fully specified name (core metadata concept)	Otodental syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15294175025) - 1237343009 -> 362991006 (116680003) View
116680003 \|Is a (attribute)\|	362991006 \|Auditory system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16374490023) - 1237343009 -> 788953003 (116680003) View
116680003 \|Is a (attribute)\|	788953003 \|Hereditary hearing loss (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294171023) - 1237343009 -> 103276001 (116680003) View
116680003 \|Is a (attribute)\|	103276001 \|Decreased hearing (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294172027) - 1237343009 -> 1083811000119108 (116680003) View
116680003 \|Is a (attribute)\|	1083811000119108 \|High frequency sensorineural hearing loss of bilateral ears (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294173021) - 1237343009 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294174026) - 1237343009 -> 1148766007 (116680003) View
116680003 \|Is a (attribute)\|	1148766007 \|Hereditary disorder of tooth (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294176029) - 1237343009 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294177022) - 1237343009 -> 707310009 (116680003) View
116680003 \|Is a (attribute)\|	707310009 \|Globodontia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294178028) - 1237343009 -> 73401004 (363698007) View
363698007 \|Finding site (attribute)\|	73401004 \|Left inner ear structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294179020) - 1237343009 -> 76473007 (363698007) View
363698007 \|Finding site (attribute)\|	76473007 \|Right inner ear structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294180023) - 1237343009 -> 47078008 (363714003) View
363714003 \|Interprets (attribute)\|	47078008 \|Hearing, function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294181022) - 1237343009 -> 1250004 (363713009) View
363713009 \|Has interpretation (attribute)\|	1250004 \|Decreased (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294182026) - 1237343009 -> 38199008 (363698007) View
363698007 \|Finding site (attribute)\|	38199008 \|Tooth structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294183020) - 1237343009 -> 442021009 (116676008) View
116676008 \|Associated morphology (attribute)\|	442021009 \|Enlargement (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15294184025) - 1237343009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	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
707310009 View
707310009	Globodontia (disorder)	Globodontia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1148766007 View
1148766007	Hereditary disorder of tooth (disorder)	Hereditary disorder of tooth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1083811000119108 View
1083811000119108	High frequency sensorineural hearing loss of bilateral ears (disorder)	High tone sensorineural hearing loss of both ears	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
103276001 View
103276001	Decreased hearing (finding)	Nghe kém	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

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 (2c00f1b4-7f55-5165-aaf8-3c4382f3102a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K00.2	TRUE	ALWAYS K00.2 \| 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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