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Terminology chevron_right Concepts chevron_right 764457005

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764457005
The component that hold information about this concept.
Cardiac arrhythmia ankyrin-b related (disorder)
Ankyrin-b 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

Cardiac arrhythmia ankyrin-b related (disorder)

SCTID: 764457005, Primitive, Active


764457005|Cardiac arrhythmia ankyrin-b related (disorder)|
  • en Ankyrin-b syndrome
  • en Cardiac arrhythmia ankyrin-b related
  • en Cardiac arrhythmia ankyrin-b related (disorder)

764457005 |Cardiac arrhythmia ankyrin-b related (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    363005004 |Cardiovascular system hereditary disorder (disorder)| +
    698270004 |Cardiac arrhythmia associated with genetic disorder (disorder)| +
    762228008 |Congenital cardiovascular disorder (disorder)| :
        { 363698007 |Finding site (attribute)| = 80891009 |Heart structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 24964005 |Cardiac conducting system structure (body structure)| }
Active

3649922019 - Ankyrin-B syndrome (en) View

3649922019
en
Synonym (core metadata concept)
Ankyrin-B syndrome
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3649921014 - Cardiac arrhythmia ankyrin-B related (en) View

3649921014
en
Synonym (core metadata concept)
Cardiac arrhythmia ankyrin-B related
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3649923012 - Cardiac arrhythmia ankyrin-B related (disorder) (en) View

3649923012
en
Fully specified name (core metadata concept)
Cardiac arrhythmia ankyrin-B related (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

Relationship (15769046020) - 764457005 -> 24964005 (363698007) View

363698007 |Finding site (attribute)|
24964005 |Cardiac conducting system structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9182170022) - 764457005 -> 11164009 (116680003) View

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

Relationship (9182171021) - 764457005 -> 363005004 (116680003) View

116680003 |Is a (attribute)|
363005004 |Cardiovascular system hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9182172025) - 764457005 -> 698270004 (116680003) View

116680003 |Is a (attribute)|
698270004 |Cardiac arrhythmia associated with genetic disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9182173024) - 764457005 -> 762228008 (116680003) View

116680003 |Is a (attribute)|
762228008 |Congenital cardiovascular disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9182174029) - 764457005 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9182175028) - 764457005 -> 80891009 (363698007) View

363698007 |Finding site (attribute)|
80891009 |Heart structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

762228008 View

762228008
Congenital cardiovascular disorder (disorder)
Congenital cardiovascular disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

698270004 View

698270004
Cardiac arrhythmia associated with genetic disorder (disorder)
Cardiac arrhythmia associated with genetic disorder
900000000000074008 |Necessary but not sufficient concept 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

363005004 View

363005004
Cardiovascular system hereditary disorder (disorder)
Cardiovascular system hereditary disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (8db7b06b-78b5-572d-9fd7-4148c37c2b87) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
I49.8
TRUE
ALWAYS I49.8
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)|
esc