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
MESH D006950

Key figures

Sex All Female Male
Number of individuals 391 125 266
Unadjusted prevalence (%) 0.22 0.13 0.35
Mean age at first event (years) 54.66 56.22 53.93
Case fatality at 5-years (%) 2.81 3.2 2.63

Longitudinal metrics

Sex All Female Male
Median nb. of events per indiv. 1 1 1
Recurrence at 6 months (%) 24.55 23.2 25.19

Associations

Loading associations…