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Details
Link-It Detail - Human Phenotype - Abnormal glucose homeostasis
Debug Stats
  • ### Total Build Time: 52 ms 27.938 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 203 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 204 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 471 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.688 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.186 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=42 ms Completed: 42 ms rowSize= 22.039 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal glucose homeostasis HP:0011014
Definition (1)
Abnormality of `glucose homeostasis` (GO:0042593).
Parents (1)
img Abnormality of carbohydrate metabolism/homeostasis HP:0011013
Children (8)
img Abnormality of blood glucose concentration HP:0011015
img Insulin insensitivity HP:0008189
img Abnormal glucose tolerance HP:0001952
img Hyperinsulinemia HP:0000842
img Abnormality of urine glucose concentration HP:0011016
img Diabetes mellitus HP:0000819
img Impaired gluconeogenesis HP:0005959
img Insulin resistance HP:0000855
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of carbohydrate metabolism/homeostasis HP:0011013
Genes (328)

Species:
human : 328
Page Size
Current 25
  Page 1 of 14
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL11P15P14100240736Chromosome 11p15-p14 deletion syndrome
img HP RolledUp, OMIM ID: 606528
HumanNIDDM4100188782Diabetes mellitus, noninsulin-dependent
img HP RolledUp, OMIM ID: 125853
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanDUPC1780895Dupuytren contracture 1
img HP RolledUp, OMIM ID: 126900
HumanGCCD3619477glucocorticoid deficiency 3
HumanCISD2493856CDGSH iron sulfur domain 2
img HP RolledUp, OMIM ID: 604928
HumanCOA5493753cytochrome c oxidase assembly factor 5
img HP RolledUp, OMIM ID: 220110
HumanSLC16A12387700solute carrier family 16, member 12
img HP RolledUp, OMIM ID: 612018
HumanLCRB387281locus control region, beta
img HP RolledUp, OMIM ID: 613985
HumanZFP57346171ZFP57 zinc finger protein
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanKCTD1284252potassium channel tetramerization domain containing 1
img HP RolledUp, OMIM ID: 181270
HumanPTRF284119polymerase I and transcript release factor
img HP RolledUp, OMIM ID: 613327
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanGCCD2282631Glucocorticoid deficiency 2
HumanPTF1A256297pancreas specific transcription factor, 1a
img HP RolledUp, OMIM ID: 609069
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanGLIS3169792GLIS family zinc finger 3
img HP RolledUp, OMIM ID: 610199
HumanSLC30A8169026solute carrier family 30 (zinc transporter), member 8
img HP RolledUp, OMIM ID: 125853
HumanBBS12166379Bardet-Biedl syndrome 12
img HP RolledUp, OMIM ID: 209900
HumanLIPI149998lipase, member I
img HP RolledUp, OMIM ID: 145750
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP RolledUp, OMIM ID: 176270
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011014Abnormal glucose homeostasis0self