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Terminology chevron_right Concepts chevron_right 1156823006

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1156823006
The component that hold information about this concept.
Autosomal recessive bilateral optic atrophy (disorder)
Autosomal recessive bilateral 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

Autosomal recessive bilateral optic atrophy (disorder)

SCTID: 1156823006, Defined, Active


1156823006|Autosomal recessive bilateral optic atrophy (disorder)|
  • en Autosomal recessive bilateral optic atrophy
  • en Autosomal recessive bilateral optic atrophy (disorder)

1156823006 |Autosomal recessive bilateral optic atrophy (disorder)|

=== 85995004 |Autosomal recessive hereditary disorder (disorder)| +
    15699081000119101 |Hereditary bilateral optic atrophy (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 68616007 |Primary atrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 724379002 |Structure of left optic nerve (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 68616007 |Primary atrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 724380004 |Structure of right optic nerve (body structure)| }
Active

4578703010 - Autosomal recessive bilateral optic atrophy (en) View

4578703010
en
Synonym (core metadata concept)
Autosomal recessive bilateral optic atrophy
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

4578702017 - Autosomal recessive bilateral optic atrophy (disorder) (en) View

4578702017
en
Fully specified name (core metadata concept)
Autosomal recessive bilateral optic atrophy (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (13820257028) - 1156823006 -> 68616007 (116676008) View

116676008 |Associated morphology (attribute)|
68616007 |Primary atrophy (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13820259025) - 1156823006 -> 85995004 (116680003) View

116680003 |Is a (attribute)|
85995004 |Autosomal recessive hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13825204027) - 1156823006 -> 15699081000119101 (116680003) View

116680003 |Is a (attribute)|
15699081000119101 |Hereditary bilateral optic atrophy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13825205026) - 1156823006 -> 724379002 (363698007) View

363698007 |Finding site (attribute)|
724379002 |Structure of left optic nerve (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13825206025) - 1156823006 -> 68616007 (116676008) View

116676008 |Associated morphology (attribute)|
68616007 |Primary atrophy (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13825207023) - 1156823006 -> 724380004 (363698007) View

363698007 |Finding site (attribute)|
724380004 |Structure of right optic nerve (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

15699081000119101 View

15699081000119101
Hereditary bilateral optic atrophy (disorder)
Hereditary bilateral optic atrophy
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

85995004 View

85995004
Autosomal recessive hereditary disorder (disorder)
Hereditary disorder trait, nos
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (e5ee7644-13a3-56db-aca3-490e35865f59) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
H47.2
TRUE
ALWAYS H47.2
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)|
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