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Terminology chevron_right Concepts chevron_right 723557004

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723557004
The component that hold information about this concept.
Thiamine-responsive encephalopathy (disorder)
Thiamine-responsive encephalopathy
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

Thiamine-responsive encephalopathy (disorder)

SCTID: 723557004, Primitive, Active


723557004|Thiamine-responsive encephalopathy (disorder)|
  • en Thiamine-responsive encephalopathy
  • en Thiamine-responsive encephalopathy (disorder)

723557004 |Thiamine-responsive encephalopathy (disorder)|

<<< 81308009 |Disorder of brain (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    128190004 |Inherited metabolic disorder of nervous system (disorder)| :
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

3425105013 - Thiamine-responsive encephalopathy (en) View

3425105013
en
Synonym (core metadata concept)
Thiamine-responsive encephalopathy
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3425104012 - Thiamine-responsive encephalopathy (disorder) (en) View

3425104012
en
Fully specified name (core metadata concept)
Thiamine-responsive encephalopathy (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
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

81308009 View

81308009
Disorder of brain (disorder)
Encephalopathy
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

ExtendedMap object (2f8f66f9-895c-5e86-b34d-11e0d25e8e8d) View

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

ExtendedMap object (b8061d84-9d5f-51d8-b99a-8db33b728eec) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G94.8
TRUE
ALWAYS G94.8 | THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
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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