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Terminology chevron_right Concepts chevron_right 722990003

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722990003
The component that hold information about this concept.
Congenital atrophy of optic nerve (disorder)
Congenital optic atrophy
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

Congenital atrophy of optic nerve (disorder)

SCTID: 722990003, Defined, Active


722990003|Congenital atrophy of optic nerve (disorder)|
  • en Congenital atrophy of optic nerve
  • en Congenital atrophy of optic nerve (disorder)
  • en Congenital optic atrophy

722990003 |Congenital atrophy of optic nerve (disorder)|

=== 66091009 |Congenital disease (disorder)| +
    76976005 |Optic atrophy (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 13331008 |Atrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 18234004 |Optic nerve structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

3334097010 - Congenital atrophy of optic nerve (en) View

3334097010
en
Synonym (core metadata concept)
Congenital atrophy of optic nerve
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3334096018 - Congenital atrophy of optic nerve (disorder) (en) View

3334096018
en
Fully specified name (core metadata concept)
Congenital atrophy of optic nerve (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3334098017 - Congenital optic atrophy (en) View

3334098017
en
Synonym (core metadata concept)
Congenital optic atrophy
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

76976005 View

76976005
Optic atrophy (disorder)
Teo thị giác
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

66091009 View

66091009
Congenital disease (disorder)
Congenital disease
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

1237618009 View

1237618009
Short stature, optic nerve atrophy, pelger-huët anomaly syndrome (disorder)
Short stature, optic nerve atrophy, pelger-huët anomaly syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

1142031005 View

1142031005
Optic atrophy due to late congenital syphilis (disorder)
Late congenital syphilitic optic atrophy
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

770625006 View

770625006
Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder)
Roifman chitayat syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

726031001 View

726031001
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder)
Camos syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

734022008 View

734022008
Wolfram-like syndrome (disorder)
Wolfram-like syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

719430008 View

719430008
Leber plus disease (disorder)
Leber plus disease
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

721200000 View

721200000
Early-onset x-linked optic atrophy (disorder)
Optic atrophy type 2
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

722213009 View

722213009
Severe x-linked intellectual disability gustavson type (disorder)
Severe x-linked intellectual disability gustavson type
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (5a5dfb63-8092-5ad8-9b79-0891c7daf1ec) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q07.8
TRUE
ALWAYS Q07.8
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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