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Terminology chevron_right Concepts chevron_right 1351572006

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1351572006
The component that hold information about this concept.
Autosomal recessive hyperimmunoglobulin m syndrome due to activation induced cytidine deaminase deficiency (disorder)
Autosomal recessive hyper-igm syndrome type 2
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 activation induced cytidine deaminase deficiency (disorder)

SCTID: 1351572006, Primitive, Active


1351572006|Autosomal recessive hyperimmunoglobulin m syndrome due to activation induced cytidine deaminase deficiency (disorder)|
  • en Autosomal recessive activation-induced cytidine deaminase deficiency
  • en Autosomal recessive hyper igm syndrome due to aicda
  • en Autosomal recessive hyper-igm syndrome type 2
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to activation induced cytidine deaminase deficiency
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to activation induced cytidine deaminase deficiency (disorder)
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to aid deficiency

1351572006 |Autosomal recessive hyperimmunoglobulin m syndrome due to activation induced cytidine deaminase deficiency (disorder)|

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

5407837018 - Autosomal recessive activation-induced cytidine deaminase deficiency (en) View

5407837018
en
Synonym (core metadata concept)
Autosomal recessive activation-induced cytidine deaminase deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

5407839015 - Autosomal recessive hyper IgM syndrome due to AICDA (en) View

5407839015
en
Synonym (core metadata concept)
Autosomal recessive hyper IgM syndrome due to AICDA
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

5407836010 - Autosomal recessive hyper-IgM syndrome type 2 (en) View

5407836010
en
Synonym (core metadata concept)
Autosomal recessive hyper-IgM syndrome type 2
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

5407838011 - Autosomal recessive hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency (en) View

5407838011
en
Synonym (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

5407834013 - Autosomal recessive hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency (disorder) (en) View

5407834013
en
Fully specified name (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to activation induced cytidine deaminase deficiency (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

5407835014 - Autosomal recessive hyperimmunoglobulin M syndrome due to AID deficiency (en) View

5407835014
en
Synonym (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to AID deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
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 (f8fe303b-4dff-5290-90eb-31ad8c95cc88) 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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