Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 1259473000

Production
add
1259473000
The component that hold information about this concept.
Dementia due to fragile x syndrome (disorder)
Dementia due to fragile x 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 due to fragile x syndrome (disorder)

SCTID: 1259473000, Defined, Active


1259473000|Dementia due to fragile x syndrome (disorder)|
  • en Dementia due to fragile x syndrome
  • en Dementia due to fragile x syndrome (disorder)

1259473000 |Dementia due to fragile x syndrome (disorder)|

=== 722980006 |Dementia due to chromosomal anomaly (disorder)| +
    1259476008 |Dementia due to genetic disease (disorder)| :
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
          363714003 |Interprets (attribute)| = 311465003 |Cognitive functions (observable entity)| }
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
        { 42752001 |Due to (attribute)| = 613003 |Fragile x syndrome (disorder)| }
Active

5159446019 - Dementia due to fragile X syndrome (en) View

5159446019
en
Synonym (core metadata concept)
Dementia due to fragile X syndrome
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

5157110012 - Dementia due to fragile X syndrome (disorder) (en) View

5157110012
en
Fully specified name (core metadata concept)
Dementia due to fragile X syndrome (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

1259476008 View

1259476008
Dementia due to genetic disease (disorder)
Dementia due to genetic disease
900000000000073002 |Sufficiently defined by necessary conditions definition status (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

ExtendedMap object (4c660921-61d3-5627-bdeb-f26dbfdcce34) 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)|

ExtendedMap object (cb97a0a9-5636-5857-a0d6-9f87b6fc844a) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q99.2
TRUE
ALWAYS Q99.2
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