Preferred Label : hyperlipidemia, familial combined;
MeSH definition : 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.;
MeSH synonym : familial combined hyperlipidemias; combined hyperlipidemias, familial; combined hyperlipidemia, familial; hyperlipidemia, multiple lipoprotein-type; multiple lipoprotein-type hyperlipidemia; lipoprotein-type hyperlipidemias, multiple; hyperlipidemia, multiple lipoprotein type; hyperlipidemias, multiple lipoprotein-type; lipoprotein-type hyperlipidemia, multiple; multiple lipoprotein-type hyperlipidemias; familial combined hyperlipidemia; hyperlipidemias, familial combined;
Wikipedia link : https://en.wikipedia.org/wiki/Hyperlipidemia, familial combined;
Origin ID : D006950;
UMLS CUI : C0020474;
Allowable qualifiers
Automatic exact mappings (from CISMeF team)
CISMeF manual mappings
Currated CISMeF NLP mapping
DO Cross reference
HPO term
Manual NTBT mappings (CISMeF)
Record concept(s)
Related MeSH Supplementary Concept(s)
See also inter- (CISMeF)
Semantic type(s)
UMLS correspondences (same concept)
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.