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Details
Link-It Detail - Disease - Hypoglycemia
Debug Stats
  • ### Total Build Time: 128 ms 47.871 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 322 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 438 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=5 ms Completed: 5 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 564 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 994 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.527 KB
  • CONCEPT_RELATIONSHIPS gt=98 ms Completed: 98 ms rowSize= 15.062 KB
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 27.661 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypoglycemia C0020615
Definition (1)
syndrome of abnormally low blood glucose level; clinical hypoglycemia has diverse etiologies; severe hypoglycemia eventually lead to glucose deprivation of the central nervous system resulting in hunger, sweating, paresthesia, impaired mental function, seizures, coma, and even death.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Glucose Metabolism Disorders C1257958
Children (2)
img Insulin Coma C0021645
img Congenital Hyperinsulinism C1257959
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Glucose Metabolism Disorders C1257958
Relationships (173)

Relation Types:
diso_​to_​anat : 13
diso_​to_​chem : 67
diso_​to_​diso : 81
diso_​to_​gene : 4
diso_​to_​phen : 2
diso_​to_​phys : 6


Relationships:
none : 98
associated_​with : 1
classifies : 1
clinically_​similar : 1
disease_​has_​finding : 2
gene_​associated_​with_​disease : 4
isa : 14
mapped_​to : 16
may_​treat : 34
parent_​is_​cdrh : 1
related_​to : 1
Page Size
Current 25
  Page 1 of 7
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO452img chemically induced C0007994
DISO_to_ANAT398img In Blood C0005768
DISO_to_CHEM378img Insulin C0021641
DISO_to_CHEM372img Agents, Antihyperglycemic C0020616
DISO_to_DISO362img Diabetes Mellitus, Insulin-Dependent C0011854
DISO_to_CHEM357img Blood Glucose C0005802
DISO_to_DISO313img chemically induced C0007994
DISO_to_DISO270img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_DISO269img Diabetes Mellitus, Insulin-Dependent C0011854
DISO_to_DISO256img Complication Aspects C1171258
DISO_to_CHEM230img Insulin C0021641
DISO_to_ANAT227img In Blood C0005768
DISO_to_DISO183img Hyperglycemia C0020456
DISO_to_DISO170img Complication Aspects C1171258
DISO_to_CHEM162img Agents, Antihyperglycemic C0020616
DISO_to_CHEM152img Blood Glucose C0005802
DISO_to_DISO98img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_DISO97img Diabetes Mellitus C0011849
DISO_to_DISO84img HYPERINSULINEMIA C0020459
DISO_to_CHEM79img Glucose C0017725
DISO_to_CHEM78img Glucose C0017725
DISO_to_DISO76img HYPERINSULINEMIA C0020459
DISO_to_DISO72img Diabetes Mellitus C0011849
DISO_to_PHEN72img genetic aspects C0017399
DISO_to_DISO61img Hyperglycemia C0020456
Genes (72)

Species:
human : 72
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanHPE6117190holoprosencephaly 6
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanNDUFAF291942NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanC20orf779133
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanMCCC156922methylcrotonoyl-CoA carboxylase 1 (alpha)
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanC10orf256652chromosome 10 open reading frame 2
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanMRAP56246melanocortin 2 receptor accessory protein
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanPNPO55163pyridoxamine 5'-phosphate oxidase
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanNDUFAF429078NADH dehydrogenase (ubiquinone) complex I, assembly factor 4
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanACAD928976acyl-CoA dehydrogenase family, member 9
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanUQCRQ27089ubiquinol-cytochrome c reductase, complex III subunit VII, 9.5kDa
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanMLYCD23417malonyl-CoA decarboxylase
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
img GENERIF, Score=827, Pubmed Id: 18547236, UMLKSK CUI: C0020615
HumanSUCLA28803succinate-CoA ligase, ADP-forming, beta subunit
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanVEGFA7422vascular endothelial growth factor A
img GENERIF, Score=1000, Pubmed Id: 18078864, UMLKSK CUI: C0020615
HumanUQCRB7381ubiquinol-cytochrome c reductase binding protein
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanTNF7124tumor necrosis factor
img GENERIF, Score=1000, Pubmed Id: 12849705, UMLKSK CUI: C0020615
HumanTK27084thymidine kinase 2, mitochondrial
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanABCC86833ATP-binding cassette, sub-family C (CFTR/MRP), member 8
img OMIM, Score=1000, UMLKSK CUI: C0020615
img OMIM, Score=1000, UMLKSK CUI: C0020615
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanSLC22A56584solute carrier family 22 (organic cation/carnitine transporter), member 5
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanSLC16A16566solute carrier family 16 (monocarboxylate transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C0020615
img OMIM, Score=1000, UMLKSK CUI: C0020615
img GENERIF, Score=861, Pubmed Id: 17701893, UMLKSK CUI: C0020615
HumanSLC2A46517solute carrier family 2 (facilitated glucose transporter), member 4
img GENERIF, Score=1000, Pubmed Id: 12064911, UMLKSK CUI: C0020615
HumanSLC2A36515solute carrier family 2 (facilitated glucose transporter), member 3
img GENERIF, Score=1000, Pubmed Id: 12064911, UMLKSK CUI: C0020615
HumanSLC2A16513solute carrier family 2 (facilitated glucose transporter), member 1
img GENERIF, Score=1000, Pubmed Id: 12064911, UMLKSK CUI: C0020615
HumanPCSK15122proprotein convertase subtilisin/kexin type 1
img OMIM, Score=1000, UMLKSK CUI: C0020615
HumanPCCB5096propionyl CoA carboxylase, beta polypeptide
img OMIM, Score=1000, UMLKSK CUI: C0020615
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020615Hypoglycemia0self