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Terminology chevron_right Concepts chevron_right 1234911006

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1234911006
The component that hold information about this concept.
Congenital cochleovestibular malformation (disorder)
Congenital cochleovestibular malformation
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

Congenital cochleovestibular malformation (disorder)

SCTID: 1234911006, Primitive, Active


1234911006|Congenital cochleovestibular malformation (disorder)|
  • en Congenital cochleovestibular malformation
  • en Congenital cochleovestibular malformation (disorder)

1234911006 |Congenital cochleovestibular malformation (disorder)|

<<< 103276001 |Decreased hearing (finding)| +
    111339003 |Congenital anomaly of ear with impairment of hearing (disorder)| +
    43353004 |Congenital anomaly of inner ear (disorder)| +
    700453005 |Congenital sensorineural hearing loss (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 22945000 |Inner ear structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          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)| }
Active

5084709014 - Congenital cochleovestibular malformation (en) View

5084709014
en
Synonym (core metadata concept)
Congenital cochleovestibular malformation
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

5084710016 - Congenital cochleovestibular malformation (disorder) (en) View

5084710016
en
Fully specified name (core metadata concept)
Congenital cochleovestibular malformation (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (15267091028) - 1234911006 -> 103276001 (116680003) View

116680003 |Is a (attribute)|
103276001 |Decreased hearing (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15267092024) - 1234911006 -> 111339003 (116680003) View

116680003 |Is a (attribute)|
111339003 |Congenital anomaly of ear with impairment of hearing (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15267093025) - 1234911006 -> 43353004 (116680003) View

116680003 |Is a (attribute)|
43353004 |Congenital anomaly of inner ear (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15267094020) - 1234911006 -> 700453005 (116680003) View

116680003 |Is a (attribute)|
700453005 |Congenital sensorineural hearing loss (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15267095021) - 1234911006 -> 47078008 (363714003) View

363714003 |Interprets (attribute)|
47078008 |Hearing, function (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15267096022) - 1234911006 -> 1250004 (363713009) View

363713009 |Has interpretation (attribute)|
1250004 |Decreased (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15267097029) - 1234911006 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15267098023) - 1234911006 -> 22945000 (363698007) View

363698007 |Finding site (attribute)|
22945000 |Inner ear structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15267099026) - 1234911006 -> 49755003 (116676008) View

116676008 |Associated morphology (attribute)|
49755003 |Morphologically abnormal structure (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15267100023) - 1234911006 -> 308490002 (370135005) View

370135005 |Pathological process (attribute)|
308490002 |Pathological developmental process (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

700453005 View

700453005
Congenital sensorineural hearing loss (disorder)
Congenital sensorineural deafness
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

111339003 View

111339003
Congenital anomaly of ear with impairment of hearing (disorder)
Congenital anomaly of ear with impairment of hearing
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

43353004 View

43353004
Congenital anomaly of inner ear (disorder)
Congenital anomaly of inner ear
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (74afa339-c88c-5396-a0fa-8b2e01972ff8) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q16.5
TRUE
ALWAYS Q16.5 | 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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