Hyperlipidemia, combined, 1

MONDO:0011237

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

Also known as: USF1 familial combined hyperlipidemia, familial combined hyperlipidemia caused by mutation in USF1, hyperlipidemia, combined, 1, hyperlipidemia, combined, type 1, hyperlipidemia, familial combined, susceptibility to, hyperlipidemia, familial combined, 1, hyplip1

0 clinical trials for this condition and its sub-types, 0 tagged with Hyperlipidemia, combined, 1 itself.

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↑ Inherited disease susceptibility (1314)

Including sub-types (0) Tagged with Hyperlipidemia, combined, 1 (0)

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