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Details
Link-It Detail - Human Phenotype - Abnormality of blood glucose concentration
Debug Stats
  • ### Total Build Time: 38 ms 25.926 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 217 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 243 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 449 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 751 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.164 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=28 ms Completed: 28 ms rowSize= 21.960 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.036 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of blood glucose concentration HP:0011015
Definition (1)
An abnormality of the concentration of `glucose` (CHEBI:17234) in the `blood` (FMA:9670).
Parents (1)
img Abnormal glucose homeostasis HP:0011014
Children (2)
img Hypoglycemia HP:0001943
img Hyperglycemia HP:0003074
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormal glucose homeostasis HP:0011014
Genes (144)

Species:
human : 144
Page Size
Current 25
  Page 1 of 6
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL11P15P14100240736Chromosome 11p15-p14 deletion syndrome
img HP RolledUp, OMIM ID: 606528
HumanGCCD3619477glucocorticoid deficiency 3
HumanZFP57346171ZFP57 zinc finger protein
img HP RolledUp, OMIM ID: 601410
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanGCCD2282631Glucocorticoid deficiency 2
HumanNDUFA11126328NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 11, 14.7kDa
img HP RolledUp, OMIM ID: 252010
HumanHPE6117190holoprosencephaly 6
img HP RolledUp, OMIM ID: 236100
HumanNDUFAF291942NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
img HP RolledUp, OMIM ID: 252010
HumanLHX489884LIM homeobox 4
img HP RolledUp, OMIM ID: 262700
HumanSERAC184947serine active site containing 1
img HP RolledUp, OMIM ID: 614739
HumanNUBPL80224nucleotide binding protein-like
img HP RolledUp, OMIM ID: 252010
HumanNDUFAF579133NADH dehydrogenase (ubiquinone) complex I, assembly factor 5
img HP RolledUp, OMIM ID: 252010
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP RolledUp, OMIM ID: 130650
img HP RolledUp, OMIM ID: 117550
HumanHYMAI57061hydatidiform mole associated and imprinted (non-protein coding)
img HP RolledUp, OMIM ID: 601410
HumanMCCC156922methylcrotonoyl-CoA carboxylase 1 (alpha)
img HP RolledUp, OMIM ID: 210200
HumanC10orf256652chromosome 10 open reading frame 2
img HP RolledUp, OMIM ID: 251880
HumanMRAP56246melanocortin 2 receptor accessory protein
HumanFOXRED155572FAD-dependent oxidoreductase domain containing 1
img HP RolledUp, OMIM ID: 252010
HumanPNPO55163pyridoxamine 5'-phosphate oxidase
img HP RolledUp, OMIM ID: 610090
HumanTTC1954902tetratricopeptide repeat domain 19
img HP RolledUp, OMIM ID: 124000
HumanMPC151660mitochondrial pyruvate carrier 1
img HP RolledUp, OMIM ID: 614741
HumanPRKAG251422protein kinase, AMP-activated, gamma 2 non-catalytic subunit
HumanNDUFAF151103NADH dehydrogenase (ubiquinone) complex I, assembly factor 1
img HP RolledUp, OMIM ID: 252010
HumanFOXP350943forkhead box P3
img HP RolledUp, OMIM ID: 222100
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011015Abnormality of blood glucose concentration0self