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Terminology chevron_right Concepts chevron_right 1351569004

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1351569004
The component that hold information about this concept.
Autosomal recessive hyperimmunoglobulin m syndrome due to uracil dna glycosylase deficiency (disorder)
Hyper-igm syndrome type 5
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

Autosomal recessive hyperimmunoglobulin m syndrome due to uracil dna glycosylase deficiency (disorder)

SCTID: 1351569004, Primitive, Active


1351569004|Autosomal recessive hyperimmunoglobulin m syndrome due to uracil dna glycosylase deficiency (disorder)|
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to ung deficiency
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to uracil dna glycosylase deficiency
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to uracil dna glycosylase deficiency (disorder)
  • en Hyper-igm syndrome due to ung
  • en Hyper-igm syndrome due to uracil n-glycosylase
  • en Hyper-igm syndrome type 5

1351569004 |Autosomal recessive hyperimmunoglobulin m syndrome due to uracil dna glycosylase deficiency (disorder)|

<<< 783249007 |Hyperimmunoglobulin m syndrome without susceptibility to opportunistic infection (disorder)| +
    403836001 |Autosomal recessive hyper- immunoglobulin m syndrome (disorder)|
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
Active

5407822017 - Autosomal recessive hyperimmunoglobulin M syndrome due to UNG deficiency (en) View

5407822017
en
Synonym (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to UNG deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

5407821012 - Autosomal recessive hyperimmunoglobulin M syndrome due to uracil DNA glycosylase deficiency (en) View

5407821012
en
Synonym (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to uracil DNA glycosylase deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

5407820013 - Autosomal recessive hyperimmunoglobulin M syndrome due to uracil DNA glycosylase deficiency (disorder) (en) View

5407820013
en
Fully specified name (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to uracil DNA glycosylase deficiency (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

5407823010 - Hyper-IgM syndrome due to UNG (en) View

5407823010
en
Synonym (core metadata concept)
Hyper-IgM syndrome due to UNG
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

5407824016 - Hyper-IgM syndrome due to uracil N-glycosylase (en) View

5407824016
en
Synonym (core metadata concept)
Hyper-IgM syndrome due to uracil N-glycosylase
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

5407830016 - Hyper-IgM syndrome type 5 (en) View

5407830016
en
Synonym (core metadata concept)
Hyper-IgM syndrome type 5
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

403836001 View

403836001
Autosomal recessive hyper- immunoglobulin m syndrome (disorder)
Autosomal recessive hyper-igm syndrome
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

783249007 View

783249007
Hyperimmunoglobulin m syndrome without susceptibility to opportunistic infection (disorder)
Hyper-igm syndrome without susceptibility to opportunistic infections
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (99753975-6887-5ac6-a0e2-d215b3d60c23) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D80.5
TRUE
ALWAYS D80.5 | 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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