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Terminology chevron_right Concepts chevron_right 1351577000

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1351577000
The component that hold information about this concept.
Autosomal recessive hyperimmunoglobulin m syndrome due to ino80 complex atpase subunit deficiency (disorder)
Hyper igm syndrome due to ino80
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 ino80 complex atpase subunit deficiency (disorder)

SCTID: 1351577000, Primitive, Active


1351577000|Autosomal recessive hyperimmunoglobulin m syndrome due to ino80 complex atpase subunit deficiency (disorder)|
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to ino80 complex atpase subunit deficiency
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to ino80 complex atpase subunit deficiency (disorder)
  • en Autosomal recessive hyperimmunoglobulin m syndrome due to ino80 deficiency
  • en Hyper igm syndrome due to ino80

1351577000 |Autosomal recessive hyperimmunoglobulin m syndrome due to ino80 complex atpase subunit deficiency (disorder)|

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

5407866015 - Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 complex ATPase subunit deficiency (en) View

5407866015
en
Synonym (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 complex ATPase subunit deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

5407863011 - Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 complex ATPase subunit deficiency (disorder) (en) View

5407863011
en
Fully specified name (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 complex ATPase subunit deficiency (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

5407864017 - Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 deficiency (en) View

5407864017
en
Synonym (core metadata concept)
Autosomal recessive hyperimmunoglobulin M syndrome due to INO80 deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

5407865016 - Hyper IgM syndrome due to INO80 (en) View

5407865016
en
Synonym (core metadata concept)
Hyper IgM syndrome due to INO80
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

Relationship (16229497020) - 1351577000 -> 403836001 (116680003) View

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

Relationship (16229498026) - 1351577000 -> 769247005 (370135005) View

370135005 |Pathological process (attribute)|
769247005 |Abnormal immune process (qualifier value)|
1
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 (5e72138c-fb62-565e-ad3a-9add8aa652f6) 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)|
esc