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Terminology chevron_right Concepts chevron_right 771471002

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771471002
The component that hold information about this concept.
Optic nerve edema, splenomegaly syndrome (disorder)
Optic nerve edema, splenomegaly syndrome
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

Optic nerve edema, splenomegaly syndrome (disorder)

SCTID: 771471002, Primitive, Active


771471002|Optic nerve edema, splenomegaly syndrome (disorder)|
  • en Optic nerve edema, splenomegaly syndrome
  • en Optic nerve edema, splenomegaly syndrome (disorder)
  • en Optic nerve oedema, splenomegaly syndrome

771471002 |Optic nerve edema, splenomegaly syndrome (disorder)|

<<< 118654009 |Disorder characterized by edema (disorder)| +
    11164009 |Autosomal dominant hereditary disorder (disorder)| +
    312942003 |Inherited optic neuropathy (disorder)| +
    16294009 |Splenomegaly (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 79654002 |Edema (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 18234004 |Optic nerve structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255398004 |Childhood (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 442021009 |Enlargement (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 181279003 |Entire spleen (body structure)| }
Active

3706355017 - Optic nerve edema, splenomegaly syndrome (en) View

3706355017
en
Synonym (core metadata concept)
Optic nerve edema, splenomegaly syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3706353012 - Optic nerve edema, splenomegaly syndrome (disorder) (en) View

3706353012
en
Fully specified name (core metadata concept)
Optic nerve edema, splenomegaly syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3706354018 - Optic nerve oedema, splenomegaly syndrome (en) View

3706354018
en
Synonym (core metadata concept)
Optic nerve oedema, splenomegaly syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (10510544027) - 771471002 -> 363343008 (116680003) View

116680003 |Is a (attribute)|
363343008 |Hereditary disorder of the visual system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (10510554028) - 771471002 -> 363235000 (116680003) View

116680003 |Is a (attribute)|
363235000 |Hereditary disorder of nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (10510545026) - 771471002 -> 16294009 (116680003) View

116680003 |Is a (attribute)|
16294009 |Splenomegaly (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10510546025) - 771471002 -> 18234004 (363698007) View

363698007 |Finding site (attribute)|
18234004 |Optic nerve structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10510547023) - 771471002 -> 79654002 (116676008) View

116676008 |Associated morphology (attribute)|
79654002 |Edema (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10510548029) - 771471002 -> 442021009 (116676008) View

116676008 |Associated morphology (attribute)|
442021009 |Enlargement (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10510549021) - 771471002 -> 11164009 (116680003) View

116680003 |Is a (attribute)|
11164009 |Autosomal dominant hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10510550021) - 771471002 -> 312942003 (116680003) View

116680003 |Is a (attribute)|
312942003 |Inherited optic neuropathy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10510551020) - 771471002 -> 255398004 (246454002) View

246454002 |Occurrence (attribute)|
255398004 |Childhood (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10510552029) - 771471002 -> 181279003 (363698007) View

363698007 |Finding site (attribute)|
181279003 |Entire spleen (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10510553023) - 771471002 -> 118654009 (116680003) View

116680003 |Is a (attribute)|
118654009 |Disorder characterized by edema (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

312942003 View

312942003
Inherited optic neuropathy (disorder)
Inherited optic neuropathy
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

16294009 View

16294009
Splenomegaly (disorder)
Lách to
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

11164009 View

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

118654009 View

118654009
Disorder characterized by edema (disorder)
Disorder characterized by edema
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True
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