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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:familial hyperlipidemia
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Accession:EFO:MONDO:0001336 term browser browse the term
Definition:An instance of hyperlipidemia (disease) that is caused by an inherited modification of the individual's genome.
Synonyms:exact_synonym: hereditary hyperlipidemia (disease)
 broad_synonym: hyperlipemia;   hyperlipidaemia
 related_synonym: familial hyperlipemia;   familial hyperlipoproteinemia
 alt_id: MONDO:0001336
 xref: DOID:1168;   ICD10CM:E78.5;   MEDGEN:675194;   MESH:D006949;   NANDO:2200603;   NCI:C34709;   SCTID:55822004;   UMLS:C0700623


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Term paths to the root
Path 1
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          metabolic disease 0
            hyperlipidemia 0
              familial hyperlipidemia 0
                cholesterol-ester transfer protein deficiency 0
                familial apolipoprotein C-II deficiency 0
                familial hypercholesterolemia + 0
                familial lipoprotein lipase deficiency 0
                hyperlipidemia due to hepatic triglyceride lipase deficiency 0
                hyperlipoproteinemia type 3 0
                hyperlipoproteinemia type V 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          genetic disorder 0
            inborn errors of metabolism 0
              inherited lipid metabolism disorder 0
                familial hyperlipidemia 0
                  cholesterol-ester transfer protein deficiency 0
                  familial apolipoprotein C-II deficiency 0
                  familial hypercholesterolemia + 0
                  familial lipoprotein lipase deficiency 0
                  hyperlipidemia due to hepatic triglyceride lipase deficiency 0
                  hyperlipoproteinemia type 3 0
                  hyperlipoproteinemia type V 0
paths to the root