hyperlipidemia, combined, 1
MONDO:0011237Mondo
Findings
No curated finding names hyperlipidemia, combined, 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An inherited susceptibility or predisposition to developing familial combined hyperlipidemia, in which the cause of the disease is a mutation in the USF1 gene.
Definition from the Mondo Disease Ontology (MONDO:0011237), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- USF1HGNC:12593
- Limited · Ambry Genetics · Autosomal dominant · 2022
Where it sits
- A kind of
Other names
4 names
Resolves to: hyperlipidemia, combined, 1
- Also called
- familial combined hyperlipidemia caused by mutation in USF1hyperlipidemia, combined, type 1hyperlipidemia, familial combined, susceptibility toUSF1 familial combined hyperlipidemia