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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) 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:hyperlipoproteinemia type IV
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Accession:DOID:1172 term browser browse the term
Definition:A hypertriglyceridemia disorder, often with autosomal dominant inheritance. It is characterized by the persistent elevations of plasma TRIGLYCERIDES, endogenously synthesized and contained predominantly in VERY-LOW-DENSITY LIPOPROTEINS (pre-beta lipoproteins). In contrast, the plasma CHOLESTEROL and PHOSPHOLIPIDS usually remain within normal limits.
Synonyms:exact_synonym: Carbohydrate Inducible Hyperlipemias;   Familial Hyperlipoproteinemia Type 4;   Familial Hypertriglyceridemia;   Familial Type IV Hyperlipoproteinemia;   Fredrickson type IV hyperlipoproteinemia;   Fredrickson type IV lipidaemia;   Fredrickson type IV lipidemia;   Hyper prebeta lipoproteinemia;   Hyperprebetalipoproteinemia;   VLDL hyperlipoproteinemia;   carbohydrate inducible hyperlipemia;   endogenous hyperlipidaemia;   type IV hyperlipoproteinemias
 primary_id: MESH:D006953
 alt_id: OMIM:144600;   OMIM:145750;   RDO:0005844
 xref: ICD10CM:E78.1;   ICD9CM:272.1;   NCI:C34711
For additional species annotation, visit the Alliance of Genome Resources.


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hyperlipoproteinemia type IV term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Apoa5 apolipoprotein A5 susceptibility ISO ClinVar Annotator: match by term: Familial hypertriglyceridemia
CTD Direct Evidence: marker/mechanism
OMIM
ClinVar
CTD
PMID:12915450, PMID:23151256, PMID:23307945, PMID:25741868 NCBI chr 8:50,559,079...50,561,720
Ensembl chr 8:50,559,126...50,561,736
JBrowse link
G Creb3l3 cAMP responsive element binding protein 3-like 3 ISO ClinVar Annotator: match by term: Familial hypertriglyceridemia ClinVar PMID:21666694 NCBI chr 7:11,490,852...11,499,287
Ensembl chr 7:11,490,852...11,499,282
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16023
    Nutritional and Metabolic Diseases 4727
      disease of metabolism 4727
        lipid metabolism disorder 899
          hyperlipoproteinemia type IV 2
Path 2
Term Annotations click to browse term
  disease 16023
    Developmental Diseases 9537
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8371
        genetic disease 7871
          inherited metabolic disorder 2237
            lipid metabolism disorder 899
              Dyslipidemias 291
                familial hyperlipidemia 267
                  Hypertriglyceridemia 94
                    hyperlipoproteinemia type IV 2
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.