Mixed hyperlipidaemia

Description

obsolete_familial combined hyperlipidemia: ['A type of familial lipid metabolism disorder characterized by a variable pattern of elevated plasma CHOLESTEROL and/or TRIGLYCERIDES. Multiple genes on different chromosomes may be involved, such as the major late transcription factor (UPSTREAM STIMULATORY FACTORS) on CHROMOSOME 1.']

Data source
FinnGen phenocode E4_HYPERLIPMIX
Hospital Discharge registry ICD-10: E782
Cause of Death registry ICD-10: E782
Level in the ICD-hierarchy 4
First defined in version DF2
Ontology
DOID 13809
GWAS catalog 0000492

Key figures

Sex All Female Male
Number of individuals 313 96 217
Unadjusted prevalence (%) 0.24 0.13 0.38
Mean age at first event (years) 55.54 57.17 54.82
Median number of events / individual 1 1 1

Clinical metrics

Sex All Female Male
Recurrence within 6 months (%) 23.32 18.75 25.35
Case fatality at 5-years (%) 3.51 4.17 3.23

Associations