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Terminology chevron_right Concepts chevron_right 403831006

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403831006
The component that hold information about this concept.
Familial hypercholesterolemia due to genetic defect of apolipoprotein b (disorder)
Familial combined hypercholesterolemia
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

Familial hypercholesterolemia due to genetic defect of apolipoprotein b (disorder)

SCTID: 403831006, Primitive, Active


403831006|Familial hypercholesterolemia due to genetic defect of apolipoprotein b (disorder)|
  • en Familial hypercholesterolaemia due to genetic defect of apolipoprotein b
  • en Familial hypercholesterolemia due to genetic defect of apolipoprotein b
  • en Familial hypercholesterolemia due to genetic defect of apolipoprotein b (disorder)
  • en Hypercholesterolaemia due to apolipoprotein b gene defect
  • en Hypercholesterolemia due to apolipoprotein b gene defect

403831006 |Familial hypercholesterolemia due to genetic defect of apolipoprotein b (disorder)|

<<< 398036000 |Familial hypercholesterolemia (disorder)| :
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
          363714003 |Interprets (attribute)| = 412808005 |Serum total cholesterol measurement (procedure)| }
Active

1784189013 - Familial Combined Hypercholesterolemia (en) View

1784189013
en
Synonym (core metadata concept)
Familial Combined Hypercholesterolemia
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
False

1783802011 - Familial Combined Hypercholesterolaemia (en) View

1783802011
en
Synonym (core metadata concept)
Familial Combined Hypercholesterolaemia
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
False

1773759012 - Familial hypercholesterolaemia due to genetic defect of apolipoprotein B (en) View

1773759012
en
Synonym (core metadata concept)
Familial hypercholesterolaemia due to genetic defect of apolipoprotein B
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

1775045012 - Familial hypercholesterolemia due to genetic defect of apolipoprotein B (en) View

1775045012
en
Synonym (core metadata concept)
Familial hypercholesterolemia due to genetic defect of apolipoprotein B
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

1771757017 - Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder) (en) View

1771757017
en
Fully specified name (core metadata concept)
Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

1783803018 - Hypercholesterolaemia due to apolipoprotein B gene defect (en) View

1783803018
en
Synonym (core metadata concept)
Hypercholesterolaemia due to apolipoprotein B gene defect
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

1784188017 - Hypercholesterolemia due to apolipoprotein B gene defect (en) View

1784188017
en
Synonym (core metadata concept)
Hypercholesterolemia due to apolipoprotein B gene defect
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

398036000 View

398036000
Familial hypercholesterolemia (disorder)
Ldl receptor disorder
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (c30b15bf-8263-566a-a303-5aeb55add675) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E78.0
TRUE
ALWAYS E78.0
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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