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Terminology chevron_right Concepts chevron_right 770434009

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770434009
The component that hold information about this concept.
Familial benign flecked retina (disorder)
Familial benign flecked retina
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

Familial benign flecked retina (disorder)

SCTID: 770434009, Primitive, Active


770434009|Familial benign flecked retina (disorder)|
  • en Familial benign flecked retina
  • en Familial benign flecked retina (disorder)

770434009 |Familial benign flecked retina (disorder)|

<<< 247138002 |Retinal flecking (disorder)| +
    41799005 |Hereditary retinal dystrophy (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 46595003 |Deposition (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
Active

3700846017 - Familial benign flecked retina (en) View

3700846017
en
Synonym (core metadata concept)
Familial benign flecked retina
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3700847014 - Familial benign flecked retina (disorder) (en) View

3700847014
en
Fully specified name (core metadata concept)
Familial benign flecked retina (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (9616860022) - 770434009 -> 85995004 (116680003) View

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

Relationship (9616861021) - 770434009 -> 5665001 (363698007) View

363698007 |Finding site (attribute)|
5665001 |Retinal structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9616863024) - 770434009 -> 41799005 (116680003) View

116680003 |Is a (attribute)|
41799005 |Hereditary retinal dystrophy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9616865028) - 770434009 -> 247138002 (116680003) View

116680003 |Is a (attribute)|
247138002 |Retinal flecking (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9616866027) - 770434009 -> 5665001 (363698007) View

363698007 |Finding site (attribute)|
5665001 |Retinal structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9633891029) - 770434009 -> 4720007 (116676008) View

116676008 |Associated morphology (attribute)|
4720007 |Dystrophy (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9633892020) - 770434009 -> 46595003 (116676008) View

116676008 |Associated morphology (attribute)|
46595003 |Deposition (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (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

85995004 View

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

247138002 View

247138002
Retinal flecking (disorder)
Retinal flecking
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (3850c419-8953-5a9f-b367-02661f18a45c) 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)|
esc