Hyperlipidaemia, other/unspecified

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_HYPERLIPNAS
Hospital Discharge registry ICD-10: E785, ICD-8: 2720[1-9]
Cause of Death registry ICD-10: E785, ICD-8: 2720[1-9]
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 2869 1254 1615
Unadjusted prevalence (%) 2.16 1.67 2.81
Mean age at first event (years) 63.39 65.14 62.04
Median number of events / individual 1 1 1

Clinical metrics

Sex All Female Male
Recurrence within 6 months (%) 17.99 18.66 17.46
Case fatality at 5-years (%) 5.58 5.1 5.94

Associations