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