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GTR Home > Conditions/Phenotypes > Hyperlipidemia, combined, 1

Summary

An inherited susceptibility or predisposition to developing familial combined hyperlipidemia, in which the cause of the disease is a mutation in the USF1 gene. [from MONDO]

Available tests

3 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: FCHL, FCHL1, HYPLIP1, MLTF, MLTFI, UEF, bHLHb11, USF1
    Summary: upstream transcription factor 1

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