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Details
Link-It Detail - Disease - Glucose Metabolism Disorders
Debug Stats
  • ### Total Build Time: 60 ms 37.984 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 354 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 445 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=1 ms Completed: 1 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= 554 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.226 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.518 KB
  • CONCEPT_RELATIONSHIPS gt=5 ms Completed: 5 ms rowSize= 12.790 KB
  • CONCEPT_GENES gt=43 ms Completed: 43 ms rowSize= 18.757 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Glucose Metabolism Disorders C1257958
Definition (1)
Pathological conditions in which the BLOOD GLUCOSE cannot be maintained within the normal range, such as in HYPOGLYCEMIA and HYPERGLYCEMIA. Etiology of these disorders varies. Plasma glucose concentration is critical to survival for it is the predominant fuel for the CENTRAL NERVOUS SYSTEM.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Metabolic Diseases C0025517
Children (5)
img Diabetes Mellitus C0011849
img Hyperinsulinism C0020459
img Glycosuria C0017979
img Hyperglycemia C0020456
img Hypoglycemia C0020615
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255173img Metabolic Diseases C0025517
Relationships (28)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 7
diso_​to_​diso : 17
diso_​to_​phen : 2


Relationships:
none : 21
entry_​version_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 4
mapped_​to : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT69img In Blood C0005768
DISO_to_DISO53img Complication Aspects C1171258
DISO_to_CHEM47img Blood Glucose C0005802
DISO_to_CHEM20img Glucose C0017725
DISO_to_DISO19img Obesity C0028754
DISO_to_PHEN17img genetic aspects C0017399
DISO_to_DISO14img Cardiovascular Diseases C0007222
DISO_to_DISO14img chemically induced C0007994
DISO_to_CHEM13img Insulin C0021641
DISO_to_DISO11img Dyslipidaemia C0242339
DISO_to_DISO11img Insulin Resistance C0021655
DISO_to_DISO10img Hypertension C0020538
DISO_to_CHEM9img ANTIPSYCHOTICS C0040615
DISO_to_DISO9img Complication Aspects C1171258
DISO_to_DISO9img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_PHEN7img genetic aspects C0017399
DISO_to_CHEM6img GLUT-1 protein C0168458
DISO_to_CHEM6img Glycosylated hemoglobin A C0019018
DISO_to_CHEM6img Hemoglobin A, Glycosylated C0019018
DISO_to_DISO6img Disease of lipid metabolism C0154251
DISO_to_DISO6img Metabolic Syndrome X C0524620
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Endocrine System C0014136
DISO_to_DISOmapped_toimg Deficiency of glyceraldehyde-3-phosphate dehydrogenase (disorder) C1291264
DISO_to_DISOisaimg Diabetes Mellitus C0011849
DISO_to_DISOentry_version_ofimg Disorder of Glucose Metabolism C1257958
Genes (670)

Species:
human : 670
Page Size
Current 25
  Page 1 of 27
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanNIDDM4100188782Diabetes mellitus, noninsulin-dependent
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanKIR2DS2100132285killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 2
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanZGLP1100125288zinc finger, GATA-like protein 1
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanSFTPA1653509surfactant protein A1
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanSUMO4387082small ubiquitin-like modifier 4
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanZFP57346171ZFP57 zinc finger protein
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanVWA2340706von Willebrand factor A domain containing 2
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanCRTC2200186CREB regulated transcription coactivator 2
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanSLC30A8169026solute carrier family 30 (zinc transporter), member 8
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanPTPRVP148713protein tyrosine phosphatase, receptor type, V, pseudogene
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanSERPINA12145264serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanPPARGC1B133522peroxisome proliferator-activated receptor gamma, coactivator 1 beta
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanPLEKHH2130271pleckstrin homology domain containing, family H (with MyTH4 domain) member 2
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanCYP2R1120227cytochrome P450, family 2, subfamily R, polypeptide 1
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanHPE6117190holoprosencephaly 6
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanAPOA5116519apolipoprotein A-V
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanGma3110204granulocyte macrophage antigen 3
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanNDUFAF291942NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanCNDP184735carnosine dipeptidase 1 (metallopeptidase M20 family)
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanGPT284706glutamic pyruvate transaminase (alanine aminotransferase) 2
INFERRED, Score=800, UMLKSK CUI: C1257958
HumanDGAT284649diacylglycerol O-acyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C1257958
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1257958Glucose Metabolism Disorders0self