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Terminology chevron_right Concepts chevron_right 783558004

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783558004
The component that hold information about this concept.
Combined oxidative phosphorylation defect type 11 (disorder)
Combined oxidative phosphorylation defect type 11
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

Combined oxidative phosphorylation defect type 11 (disorder)

SCTID: 783558004, Primitive, Active


783558004|Combined oxidative phosphorylation defect type 11 (disorder)|
  • en Combined oxidative phosphorylation defect type 11
  • en Combined oxidative phosphorylation defect type 11 (disorder)
  • en Coxpd11 - combined oxidative phosphorylation defect type 11

783558004 |Combined oxidative phosphorylation defect type 11 (disorder)|

<<< 85995004 |Autosomal recessive hereditary disorder (disorder)| +
    128190004 |Inherited metabolic disorder of nervous system (disorder)| +
    240096000 |Mitochondrial cytopathy (disorder)| :
        { 363698007 |Finding site (attribute)| = 25087005 |Structure of nervous system (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

3759344011 - Combined oxidative phosphorylation defect type 11 (en) View

3759344011
en
Synonym (core metadata concept)
Combined oxidative phosphorylation defect type 11
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3759346013 - Combined oxidative phosphorylation defect type 11 (disorder) (en) View

3759346013
en
Fully specified name (core metadata concept)
Combined oxidative phosphorylation defect type 11 (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3759345012 - COXPD11 - combined oxidative phosphorylation defect type 11 (en) View

3759345012
en
Synonym (core metadata concept)
COXPD11 - combined oxidative phosphorylation defect type 11
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

128190004 View

128190004
Inherited metabolic disorder of nervous system (disorder)
Inherited metabolic disorder of nervous system
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

240096000 View

240096000
Mitochondrial cytopathy (disorder)
Mitochondrial disease
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (583c4ce2-e3bb-571d-a9fb-137ce24973d7) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E88.8
TRUE
ALWAYS E88.8 | 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)|
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