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Terminology chevron_right Concepts chevron_right 1172602000

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1172602000
The component that hold information about this concept.
Childhood-onset benign chorea with striatal involvement (disorder)
Childhood-onset benign chorea with striatal involvement
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

Childhood-onset benign chorea with striatal involvement (disorder)

SCTID: 1172602000, Primitive, Active


1172602000|Childhood-onset benign chorea with striatal involvement (disorder)|
  • en Childhood-onset benign chorea with striatal involvement
  • en Childhood-onset benign chorea with striatal involvement (disorder)

1172602000 |Childhood-onset benign chorea with striatal involvement (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    230306001 |Benign hereditary chorea (disorder)| +
    896882009 |Structural abnormality of corpus striatum (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 31428008 |Corpus striatum structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255398004 |Childhood (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
Active

4634546010 - Childhood-onset benign chorea with striatal involvement (en) View

4634546010
en
Synonym (core metadata concept)
Childhood-onset benign chorea with striatal involvement
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

4634547018 - Childhood-onset benign chorea with striatal involvement (disorder) (en) View

4634547018
en
Fully specified name (core metadata concept)
Childhood-onset benign chorea with striatal involvement (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (16377454021) - 1172602000 -> 896882009 (116680003) View

116680003 |Is a (attribute)|
896882009 |Structural abnormality of corpus striatum (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15512997027) - 1172602000 -> 255324009 (363714003) View

363714003 |Interprets (attribute)|
255324009 |Movement (observable entity)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (14008652024) - 1172602000 -> 70835005 (116680003) View

116680003 |Is a (attribute)|
70835005 |Disorder of basal ganglia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (15502058027) - 1172602000 -> 263654008 (363713009) View

363713009 |Has interpretation (attribute)|
263654008 |Abnormal (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15512998021) - 1172602000 -> 363847004 (363714003) View

363714003 |Interprets (attribute)|
363847004 |Movement observable (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14008650027) - 1172602000 -> 11164009 (116680003) View

116680003 |Is a (attribute)|
11164009 |Autosomal dominant hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14008651028) - 1172602000 -> 230306001 (116680003) View

116680003 |Is a (attribute)|
230306001 |Benign hereditary chorea (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14008653025) - 1172602000 -> 255398004 (246454002) View

246454002 |Occurrence (attribute)|
255398004 |Childhood (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14008654020) - 1172602000 -> 31428008 (363698007) View

363698007 |Finding site (attribute)|
31428008 |Corpus striatum structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14008655021) - 1172602000 -> 49755003 (116676008) View

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

896882009 View

896882009
Structural abnormality of corpus striatum (disorder)
Abnormal corpus striatum morphology
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

230306001 View

230306001
Benign hereditary chorea (disorder)
Benign hereditary chorea
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (989b5ae6-1543-5e45-8c5f-5716bb8b73e6) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G25.5
TRUE
ALWAYS G25.5 | 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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