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Terminology chevron_right Concepts chevron_right 733194007

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733194007
The component that hold information about this concept.
Dementia co-occurrent and due to down syndrome (disorder)
Dementia with down syndrome
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

Dementia co-occurrent and due to down syndrome (disorder)

SCTID: 733194007, Defined, Active


733194007|Dementia co-occurrent and due to down syndrome (disorder)|
  • en Dementia co-occurrent and due to down syndrome
  • en Dementia co-occurrent and due to down syndrome (disorder)
  • en Dementia with down syndrome

733194007 |Dementia co-occurrent and due to down syndrome (disorder)|

=== 722980006 |Dementia due to chromosomal anomaly (disorder)| +
    41040004 |Complete trisomy 21 syndrome (disorder)| :
        { 42752001 |Due to (attribute)| = 41040004 |Complete trisomy 21 syndrome (disorder)| }
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
          363714003 |Interprets (attribute)| = 311465003 |Cognitive functions (observable entity)| }
        { 116676008 |Associated morphology (attribute)| = 78989007 |Trisomy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 43009003 |Chromosome pair 21 (cell structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
Active

3498963010 - Dementia co-occurrent and due to Down syndrome (en) View

3498963010
en
Synonym (core metadata concept)
Dementia co-occurrent and due to Down syndrome
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3498964016 - Dementia co-occurrent and due to Down syndrome (disorder) (en) View

3498964016
en
Fully specified name (core metadata concept)
Dementia co-occurrent and due to Down syndrome (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3498962017 - Dementia with Down syndrome (en) View

3498962017
en
Synonym (core metadata concept)
Dementia with Down syndrome
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

Relationship (13763565025) - 733194007 -> 308490002 (370135005) View

370135005 |Pathological process (attribute)|
308490002 |Pathological developmental process (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7079013023) - 733194007 -> 41040004 (42752001) View

42752001 |Due to (attribute)|
41040004 |Complete trisomy 21 syndrome (disorder)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7079016026) - 733194007 -> 12738006 (363698007) View

363698007 |Finding site (attribute)|
12738006 |Brain structure (body structure)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10751157020) - 733194007 -> 260379002 (363713009) View

363713009 |Has interpretation (attribute)|
260379002 |Impaired (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10751158026) - 733194007 -> 311465003 (363714003) View

363714003 |Interprets (attribute)|
311465003 |Cognitive functions (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7079014028) - 733194007 -> 41040004 (116680003) View

116680003 |Is a (attribute)|
41040004 |Complete trisomy 21 syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7079015027) - 733194007 -> 722980006 (116680003) View

116680003 |Is a (attribute)|
722980006 |Dementia due to chromosomal anomaly (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7079017024) - 733194007 -> 78989007 (116676008) View

116676008 |Associated morphology (attribute)|
78989007 |Trisomy (morphologic abnormality)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7079018025) - 733194007 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7079019022) - 733194007 -> 43009003 (363698007) View

363698007 |Finding site (attribute)|
43009003 |Chromosome pair 21 (cell structure)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

722980006 View

722980006
Dementia due to chromosomal anomaly (disorder)
Dementia due to chromosomal anomaly
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

41040004 View

41040004
Complete trisomy 21 syndrome (disorder)
Mongolism
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (1ab69214-f970-5283-a444-3ed03c95a9de) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q90.9
TRUE
ALWAYS Q90.9
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)|

ExtendedMap object (7d2bc6b2-36b7-501b-b929-f08ddd541df2) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
F02.8
TRUE
ALWAYS F02.8 | THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
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)|
esc