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Terminology chevron_right Concepts chevron_right 95844003

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95844003
The component that hold information about this concept.
Dysplasminogenemia (disorder)
Dysplasminogenemia
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

Dysplasminogenemia (disorder)

SCTID: 95844003, Primitive, Active


95844003|Dysplasminogenemia (disorder)|
  • en Dysplasminogenaemia
  • en Dysplasminogenemia
  • en Dysplasminogenemia (disorder)

95844003 |Dysplasminogenemia (disorder)|

<<< 95839005 |Disorder involving the fibrinolytic system (disorder)| :
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 74848003 |Hemostatic function (observable entity)| }
Active

512326014 - Dysplasminogenaemia (en) View

512326014
en
Synonym (core metadata concept)
Dysplasminogenaemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

158743011 - Dysplasminogenemia (en) View

158743011
en
Synonym (core metadata concept)
Dysplasminogenemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

840083014 - Dysplasminogenemia (disorder) (en) View

840083014
en
Fully specified name (core metadata concept)
Dysplasminogenemia (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (11290234023) - 95844003 -> 74848003 (363714003) View

363714003 |Interprets (attribute)|
74848003 |Hemostatic function (observable entity)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11290235024) - 95844003 -> 263654008 (363713009) View

363713009 |Has interpretation (attribute)|
263654008 |Abnormal (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (2740030023) - 95844003 -> 91689009 (363698007) View

363698007 |Finding site (attribute)|
91689009 |Body system structure (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2789435029) - 95844003 -> 128153000 (363705008) View

363705008 |Has definitional manifestation (attribute)|
128153000 |Hemostatic system finding (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (931125021) - 95844003 -> 281833003 (363698007) View

363698007 |Finding site (attribute)|
281833003 |Entire hematological system (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (307954028) - 95844003 -> 95839005 (116680003) View

116680003 |Is a (attribute)|
95839005 |Disorder involving the fibrinolytic system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

95839005 View

95839005
Disorder involving the fibrinolytic system (disorder)
Disorder of fibrinolysis
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

95845002 View

95845002
Hereditary dysplasminogenemia (disorder)
Hereditary dysplasminogenemia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (db58e58c-7c44-53f3-a6a2-acd989a813af) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D68.8
TRUE
ALWAYS D68.8 | MAPPED FOLLOWING WHO GUIDANCE
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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