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Terminology chevron_right Concepts chevron_right 1237339005

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1237339005
The component that hold information about this concept.
Severe primary trimethylaminuria (disorder)
Severe primary trimethylaminuria
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

Severe primary trimethylaminuria (disorder)

SCTID: 1237339005, Primitive, Active


1237339005|Severe primary trimethylaminuria (disorder)|
  • en Severe primary trimethylaminuria
  • en Severe primary trimethylaminuria (disorder)

1237339005 |Severe primary trimethylaminuria (disorder)|

<<< 237959005 |Trimethylaminuria (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    86095007 |Inborn error of metabolism (disorder)| :
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

5097782012 - Severe primary trimethylaminuria (en) View

5097782012
en
Synonym (core metadata concept)
Severe primary trimethylaminuria
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

5097781017 - Severe primary trimethylaminuria (disorder) (en) View

5097781017
en
Fully specified name (core metadata concept)
Severe primary trimethylaminuria (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
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

86095007 View

86095007
Inborn error of metabolism (disorder)
Inborn error of metabolism
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

237959005 View

237959005
Trimethylaminuria (disorder)
Trimethylaminuria
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (59153f0a-3e5c-5cbe-b940-f29a68924fe4) 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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