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Terminology chevron_right Concepts chevron_right 1351573001

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1351573001
The component that hold information about this concept.
Autosomal recessive hyperimmunoglobulin m syndrome due to april deficiency (disorder)
Hyper igm syndrome due to tnfsf13
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 april deficiency (disorder)

SCTID: 1351573001, Primitive, Active


1351573001|Autosomal recessive hyperimmunoglobulin m syndrome due to april deficiency (disorder)|
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to april deficiency
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to april deficiency (disorder)
  • en Hyper igm syndrome due to tnfsf13

1351573001 |Autosomal recessive hyperimmunoglobulin m syndrome due to april deficiency (disorder)|

<<< 403836001 |Autosomal recessive hyper- immunoglobulin m syndrome (disorder)|
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
Active

5407841019 - Autosomal recessive hyperimmunoglobulin M syndrome due to APRIL deficiency (en) View

5407841019
en
Synonym (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to APRIL deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

5407843016 - Autosomal recessive hyperimmunoglobulin M syndrome due to APRIL deficiency (disorder) (en) View

5407843016
en
Fully specified name (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to APRIL deficiency (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

5407842014 - Hyper IgM syndrome due to TNFSF13 (en) View

5407842014
en
Synonym (core metadata concept)
Hyper IgM syndrome due to TNFSF13
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

Relationship (16229478020) - 1351573001 -> 403836001 (116680003) View

116680003 |Is a (attribute)|
403836001 |Autosomal recessive hyper- immunoglobulin m syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (16229480025) - 1351573001 -> 769247005 (370135005) View

370135005 |Pathological process (attribute)|
769247005 |Abnormal immune process (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
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

ExtendedMap object (d12a1c4a-1750-589c-83e8-4ff7f28c04ae) 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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