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Details
Link-It Detail - Disease - Hyperinsulinism
Debug Stats
  • ### Total Build Time: 169 ms 38.661 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 496 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=0 Completed: 0 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=16 ms Completed: 16 ms rowSize= 564 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 1,000 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.527 KB
  • CONCEPT_RELATIONSHIPS gt=84 ms Completed: 84 ms rowSize= 13.013 KB
  • CONCEPT_GENES gt=51 ms Completed: 51 ms rowSize= 20.429 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperinsulinism C0020459
Definition (1)
A syndrome with excessively high INSULIN levels in the BLOOD. It may cause HYPOGLYCEMIA. Etiology of hyperinsulinism varies, including hypersecretion of a beta cell tumor (INSULINOMA); autoantibodies against insulin (INSULIN ANTIBODIES); defective insulin receptor (INSULIN RESISTANCE); or overuse of exogenous insulin or HYPOGLYCEMIC AGENTS.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Glucose Metabolism Disorders C1257958
Children (2)
img Congenital Hyperinsulinism C1257959
img Insulin Resistance C0021655
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Glucose Metabolism Disorders C1257958
Relationships (89)

Relation Types:
diso_​to_​anat : 9
diso_​to_​chem : 23
diso_​to_​diso : 53
diso_​to_​phen : 2
diso_​to_​phys : 2


Relationships:
none : 75
isa : 10
mapped_​to : 3
use : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT158img In Blood C0005768
DISO_to_ANAT151img In Blood C0005768
DISO_to_DISO151img Complication Aspects C1171258
DISO_to_DISO141img Complication Aspects C1171258
DISO_to_DISO121img Insulin Resistance C0021655
DISO_to_CHEM120img Insulin C0021641
DISO_to_CHEM98img Insulin C0021641
DISO_to_DISO88img Insulin Resistance C0021655
DISO_to_DISO84img Hypoglycemia C0020615
DISO_to_PHEN82img genetic aspects C0017399
DISO_to_DISO79img Obesity C0028754
DISO_to_DISO77img Obesity C0028754
DISO_to_DISO76img Hypoglycemia C0020615
DISO_to_PHEN72img genetic aspects C0017399
DISO_to_DISO62img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_DISO48img chemically induced C0007994
DISO_to_CHEM42img Agents, Antihyperglycemic C0020616
DISO_to_CHEM41img Blood Glucose C0005802
DISO_to_DISO41img Hyperglycemia C0020456
DISO_to_DISO39img Polycystic Ovary Syndrome C0032460
DISO_to_DISO37img Hyperglycemia C0020456
DISO_to_DISO37img Polycystic Ovary Syndrome C0032460
DISO_to_DISO36img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_CHEM35img Agents, Antihyperglycemic C0020616
DISO_to_CHEM31img Blood Glucose C0005802
Genes (204)

Species:
human : 204
Page Size
Current 25
  Page 1 of 9
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNIDDM4100188782Diabetes mellitus, noninsulin-dependent
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanSFTPA1653509surfactant protein A1
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanSLC30A8169026solute carrier family 30 (zinc transporter), member 8
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanSERPINA12145264serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanAPOA5116519apolipoprotein A-V
img GENERIF, Score=1000, Pubmed Id: 15684402, UMLKSK CUI: C0020459
HumanGPT284706glutamic pyruvate transaminase (alanine aminotransferase) 2
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanDGAT284649diacylglycerol O-acyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanAKT1S184335AKT1 substrate 1 (proline-rich)
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanSTEAP479689STEAP family member 4
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanADIPOR279602adiponectin receptor 2
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanFTO79068fat mass and obesity associated
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanABCG864241ATP-binding cassette, sub-family G (WHITE), member 8
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanTRIB357761tribbles homolog 3 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanPNPLA257104patatin-like phospholipase domain containing 2
img GENERIF, Score=1000, Pubmed Id: 17356053, UMLKSK CUI: C0020459
HumanRETN56729resistin
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanSELS55829
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanITLN155600intelectin 1 (galactofuranose binding)
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanPARL55486presenilin associated, rhomboid-like
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanCDKAL154901CDK5 regulatory subunit associated protein 1-like 1
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanGHRL51738ghrelin/obestatin prepropeptide
img GENERIF, Score=1000, Pubmed Id: 15070922, UMLKSK CUI: C0020459
img GENERIF, Score=1000, Pubmed Id: 18205273, UMLKSK CUI: C0020459
HumanADIPOR151094adiponectin receptor 1
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanNIDDM350982Noninsulin-dependent diabetes mellitus 3
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
img OMIM, Score=1000, UMLKSK CUI: C0020459
HumanFGF2126291fibroblast growth factor 21
INFERRED, Score=800, UMLKSK CUI: C0020459
HumanLPIN123175lipin 1
INFERRED, Score=800, UMLKSK CUI: C0020459
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020459Hyperinsulinism0self