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Terminology chevron_right Concepts chevron_right 1351652007

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1351652007
The component that hold information about this concept.
Autosomal recessive combined immunodeficiency due to copi coat complex subunit gamma 1 deficiency (disorder)
Autosomal recessive combined immunodeficiency due to copg1 deficiency
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 combined immunodeficiency due to copi coat complex subunit gamma 1 deficiency (disorder)

SCTID: 1351652007, Primitive, Active


1351652007|Autosomal recessive combined immunodeficiency due to copi coat complex subunit gamma 1 deficiency (disorder)|
  • en Autosomal recessive combined immunodeficiency due to copg1 deficiency
  • en Autosomal recessive combined immunodeficiency due to copi coat complex subunit gamma 1 deficiency
  • en Autosomal recessive combined immunodeficiency due to copi coat complex subunit gamma 1 deficiency (disorder)

1351652007 |Autosomal recessive combined immunodeficiency due to copi coat complex subunit gamma 1 deficiency (disorder)|

<<< 442459007 |Combined immunodeficiency disease (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| :
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
Active

5408281019 - Autosomal recessive combined immunodeficiency due to COPG1 deficiency (en) View

5408281019
en
Synonym (core metadata concept)
Autosomal recessive combined immunodeficiency due to COPG1 deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

5414350014 - Autosomal recessive combined immunodeficiency due to COPI coat complex subunit gamma 1 deficiency (en) View

5414350014
en
Synonym (core metadata concept)
Autosomal recessive combined immunodeficiency due to COPI coat complex subunit gamma 1 deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

5408279016 - Autosomal recessive combined immunodeficiency due to COPI coat complex subunit gamma 1 deficiency (disorder) (en) View

5408279016
en
Fully specified name (core metadata concept)
Autosomal recessive combined immunodeficiency due to COPI coat complex subunit gamma 1 deficiency (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

442459007 View

442459007
Combined immunodeficiency disease (disorder)
Combined immunodeficiency disease
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
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

ExtendedMap object (3b6a0bb1-d768-563e-8bce-069c697025d8) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D81.8
TRUE
ALWAYS D81.8
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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