Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 716746003

Production
add
716746003
The component that hold information about this concept.
Congenital alpha-2-antiplasmin deficiency (disorder)
Congenital alpha2-antiplasmin 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

Congenital alpha-2-antiplasmin deficiency (disorder)

SCTID: 716746003, Primitive, Active


716746003|Congenital alpha-2-antiplasmin deficiency (disorder)|
  • en Congenital alpha-2-antiplasmin deficiency
  • en Congenital alpha2-antiplasmin deficiency
  • en Congenital alpha-2-antiplasmin deficiency (disorder)

716746003 |Congenital alpha-2-antiplasmin deficiency (disorder)|

<<< 66091009 |Congenital disease (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    234465007 |Alpha-2-antiplasmin deficiency (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

3307410014 - Congenital alpha-2-antiplasmin deficiency (en) View

3307410014
en
Synonym (core metadata concept)
Congenital alpha-2-antiplasmin deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3307411013 - Congenital alpha2-antiplasmin deficiency (en) View

3307411013
en
Synonym (core metadata concept)
Congenital alpha2-antiplasmin deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3307409016 - Congenital alpha-2-antiplasmin deficiency (disorder) (en) View

3307409016
en
Fully specified name (core metadata concept)
Congenital alpha-2-antiplasmin deficiency (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

66091009 View

66091009
Congenital disease (disorder)
Congenital disease
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

234465007 View

234465007
Alpha-2-antiplasmin deficiency (disorder)
Alpha-2-antiplasmin deficiency
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (1e2287ec-44e7-5737-b6a1-176811d84562) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D68.8
TRUE
ALWAYS D68.8
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)|
esc