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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:ApoA-I and ApoC-III Deficiency, Combined
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Accession:DOID:9006634 term browser browse the term
Synonyms:exact_synonym: APOA1 and APOC3 deficiency, combined
For additional species annotation, visit the Alliance of Genome Resources.

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17445
    Nutritional and Metabolic Diseases 5595
      disease of metabolism 5595
        lipid metabolism disorder 1029
          hypolipoproteinemia 15
            Hypoalphalipoproteinemias 4
              primary hypoalphalipoproteinemia 2 1
                ApoA-I and ApoC-III Deficiency, Combined 0
Path 2
Term Annotations click to browse term
  disease 17445
    Developmental Disease 11029
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9553
        genetic disease 9078
          inherited metabolic disorder 2663
            lipid metabolism disorder 1029
              Dyslipidemias 334
                familial hyperlipidemia 308
                  Hyperlipoproteinemias 68
                    cholesterol-ester transfer protein deficiency 1
                      apolipoprotein C-III deficiency 1
                        ApoA-I and ApoC-III Deficiency, Combined 0
paths to the root