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Terminology chevron_right Concepts chevron_right 711162004

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711162004
The component that hold information about this concept.
Autosomal dominant vitreoretinochoroidopathy (disorder)
Autosomal dominant vitreoretinochoroidopathy
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 vitreoretinochoroidopathy (disorder)

SCTID: 711162004, Primitive, Active


711162004|Autosomal dominant vitreoretinochoroidopathy (disorder)|
  • en Autosomal dominant vitreoretinochoroidopathy
  • en Autosomal dominant vitreoretinochoroidopathy (disorder)
  • en Autosomal dominant vitreoretinochoroidopathy with nanophthalmos
  • en Vitreoretinochoroidopathy with microcornea, glaucoma and cataract

711162004 |Autosomal dominant vitreoretinochoroidopathy (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

3047555016 - Autosomal dominant vitreoretinochoroidopathy (en) View

3047555016
en
Synonym (core metadata concept)
Autosomal dominant vitreoretinochoroidopathy
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3047554017 - Autosomal dominant vitreoretinochoroidopathy (disorder) (en) View

3047554017
en
Fully specified name (core metadata concept)
Autosomal dominant vitreoretinochoroidopathy (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3078092019 - Autosomal dominant vitreoretinochoroidopathy with nanophthalmos (en) View

3078092019
en
Synonym (core metadata concept)
Autosomal dominant vitreoretinochoroidopathy with nanophthalmos
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3078068010 - Vitreoretinochoroidopathy with microcornea, glaucoma and cataract (en) View

3078068010
en
Synonym (core metadata concept)
Vitreoretinochoroidopathy with microcornea, glaucoma and cataract
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

ExtendedMap object (cf9ed60c-24cb-58b7-9631-10e7b638ba6e) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
H35.5
TRUE
ALWAYS H35.5
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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