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Terminology chevron_right Concepts chevron_right 724344004

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724344004
The component that hold information about this concept.
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder)
Hypercoagulability syndrome due to glycosylphosphatidylinositol 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

Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder)

SCTID: 724344004, Primitive, Active


724344004|Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder)|
  • en Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
  • en Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder)

724344004 |Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder)|

<<< 85995004 |Autosomal recessive hereditary disorder (disorder)| +
    238045003 |Disorder of glycoprotein metabolism (disorder)| +
    439698008 |Hereditary thrombophilia (disorder)| :
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 74848003 |Hemostatic function (observable entity)| }
Active

3434248011 - Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (en) View

3434248011
en
Synonym (core metadata concept)
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3434247018 - Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder) (en) View

3434247018
en
Fully specified name (core metadata concept)
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

439698008 View

439698008
Hereditary thrombophilia (disorder)
Primary thrombophilia
900000000000073002 |Sufficiently defined by necessary conditions 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

238045003 View

238045003
Disorder of glycoprotein metabolism (disorder)
Glycoprotein metabolism disorder
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (0ac2067d-abf5-56e2-8040-128e28729d17) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E88.8
TRUE
ALWAYS E88.8 | 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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