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1784189013
The component that hold information about this description.
403831006 |Familial hypercholesterolemia due to genetic defect of apolipoprotein b (disorder)|
Identifies the concept to which this description applies. Set to the identifier of a concept with id 138875005
en
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900000000000013009 |Synonym (core metadata concept)|
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Familial Combined Hypercholesterolemia
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900000000000020002 |Only initial character case insensitive (core metadata concept)|
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Acceptable
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