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Details
Link-It Detail - Disease - Hyperlipoproteinemia Type IV
Debug Stats
  • ### Total Build Time: 125 ms 21.001 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 354 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 316 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=15 ms Completed: 15 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1.411 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 5.433 KB
  • CONCEPT_RELATIONSHIPS gt=72 ms Completed: 72 ms rowSize= 9.477 KB
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 2.646 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperlipoproteinemia Type IV C0020480
Definition (1)
characterized by an isolated elevation in the plasma level of endogenously synthesized triglyceride carried in VLDL; considered to be an autosomal dominant trait.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (3)
img Hypertriglyceridemia C0020557
img Hyperlipoproteinemias C0020476
img Lipid Metabolism, Inborn Errors C0023772
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255177img Hypertriglyceridemia C0020557
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255177img Hyperlipoproteinemias C0020476
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501235img Lipid Metabolism, Inborn Errors C0023772
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255175img Lipid Metabolism, Inborn Errors C0023772
Relationships (21)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 4
diso_​to_​diso : 12
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 9
classifies : 1
isa : 4
mapped_​to : 6
used_​for : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN12img genetic aspects C0017399
DISO_to_ANAT9img In Blood C0005768
DISO_to_PHEN8img genetic aspects C0017399
DISO_to_CHEM7img LIPOPROTEIN LIPASE C0023816
DISO_to_DISO7img Complication Aspects C1171258
DISO_to_ANAT4img In Blood C0005768
DISO_to_CHEM4img Apo-A C0003592
DISO_to_CHEM4img Apolipoproteins A C0003592
DISO_to_PHYS4img Mutation, Missense C0599155
DISO_to_CHEMmapped_toimg Triglycerides C0041004
DISO_to_DISOmapped_toimg Anapolipoproteinaemia C0268199
DISO_to_DISOclassifiesimg Disease of lipid metabolism C0154251
DISO_to_DISOmapped_toimg EXOGENOUS HYPERTRIGLYCERIDEMIA C0342889
DISO_to_DISOisaimg Hyperlipoproteinemia Type I C0023817
DISO_to_DISOused_forimg Hyperlipoproteinemia Type IV C0020480
DISO_to_DISOisaimg Hyperlipoproteinemia Type V C0020481
DISO_to_DISOmapped_toimg Hypertriglyceridemia C0020557
DISO_to_DISOisaimg Primary genetic hyperlipidaemia C1304448
DISO_to_DISOmapped_toimg Primary hypertriglyceridaemia C0342886
DISO_to_DISOmapped_toimg Sporadic primary hypertriglyceridaemia C1304250
DISO_to_DISOisaimg Very low density lipoprotinaemia C0342887
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanSLC10A26555solute carrier family 10 (sodium/bile acid cotransporter), member 2
img GENERIF, Score=734, Pubmed Id: 11742882, UMLKSK CUI: C0020480
HumanAPOA4337apolipoprotein A-IV
img GENERIF, Score=1000, Pubmed Id: 18664021, UMLKSK CUI: C0020480
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020480Hyperlipoproteinemia Type IV0self