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Terminology chevron_right Concepts chevron_right 719431007

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719431007
The component that hold information about this concept.
Autosomal dominant late-onset retinal degeneration (disorder)
Late-onset retinal degeneration
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

Autosomal dominant late-onset retinal degeneration (disorder)

SCTID: 719431007, Primitive, Active


719431007|Autosomal dominant late-onset retinal degeneration (disorder)|
  • en Autosomal dominant late-onset retinal degeneration
  • en Autosomal dominant late-onset retinal degeneration (disorder)
  • en Late-onset retinal degeneration

719431007 |Autosomal dominant late-onset retinal degeneration (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    41799005 |Hereditary retinal dystrophy (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
Active

3316320017 - Autosomal dominant late-onset retinal degeneration (en) View

3316320017
en
Synonym (core metadata concept)
Autosomal dominant late-onset retinal degeneration
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3315716013 - Autosomal dominant late-onset retinal degeneration (disorder) (en) View

3315716013
en
Fully specified name (core metadata concept)
Autosomal dominant late-onset retinal degeneration (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3316321018 - Late-onset retinal degeneration (en) View

3316321018
en
Synonym (core metadata concept)
Late-onset retinal degeneration
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

11164009 View

11164009
Autosomal dominant hereditary disorder (disorder)
Ad - autosomal dominant
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

41799005 View

41799005
Hereditary retinal dystrophy (disorder)
Hereditary retinal dystrophy
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True
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