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Terminology chevron_right Concepts chevron_right 732264002

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732264002
The component that hold information about this concept.
Coenzyme a synthase protein associated neurodegeneration (disorder)
Coasy protein-associated neurodegeneration
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

Coenzyme a synthase protein associated neurodegeneration (disorder)

SCTID: 732264002, Primitive, Active


732264002|Coenzyme a synthase protein associated neurodegeneration (disorder)|
  • en Coasy protein-associated neurodegeneration
  • en Coenzyme a synthase protein associated neurodegeneration
  • en Coenzyme a synthase protein associated neurodegeneration (disorder)
  • en Copan - coenzyme a synthase protein associated neurodegeneration
  • en Neurodegeneration with brain iron accumulation due to coasy mutation

732264002 |Coenzyme a synthase protein associated neurodegeneration (disorder)|

<<< 60737008 |Iron overload (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| :
        { 246075003 |Causative agent (attribute)| = 767270007 |Iron and iron compound (substance)|,
          363698007 |Finding site (attribute)| = 25087005 |Structure of nervous system (body structure)| }
Active

3465161018 - COASY protein-associated neurodegeneration (en) View

3465161018
en
Synonym (core metadata concept)
COASY protein-associated neurodegeneration
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

3465160017 - Coenzyme A synthase protein associated neurodegeneration (en) View

3465160017
en
Synonym (core metadata concept)
Coenzyme A synthase protein associated neurodegeneration
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3465159010 - Coenzyme A synthase protein associated neurodegeneration (disorder) (en) View

3465159010
en
Fully specified name (core metadata concept)
Coenzyme A synthase protein associated neurodegeneration (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3465162013 - CoPAN - coenzyme A synthase protein associated neurodegeneration (en) View

3465162013
en
Synonym (core metadata concept)
CoPAN - coenzyme A synthase protein associated neurodegeneration
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

3465163015 - Neurodegeneration with brain iron accumulation due to COASY mutation (en) View

3465163015
en
Synonym (core metadata concept)
Neurodegeneration with brain iron accumulation due to COASY mutation
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

60737008 View

60737008
Iron overload (disorder)
Iron excess
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

363235000 View

363235000
Hereditary disorder of nervous system (disorder)
Hereditary disorder of nervous system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (e9aa7ca2-58a3-5494-8520-a52a3cc34d44) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G23.0
TRUE
ALWAYS G23.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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