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Details
Link-It Detail - Disease - Congenital glucose-galactose malabsorption
Debug Stats
  • ### Total Build Time: 31 ms 9.705 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=26 ms Completed: 26 ms rowSize= 6.511 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 1.575 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Congenital glucose-galactose malabsorption C0268186
Relationships (13)

Relation Types:
diso_​to_​chem : 2
diso_​to_​diso : 11


Relationships:
associated_​with : 2
clinically_​similar : 1
expanded_​form_​of : 1
isa : 1
manifestation_​of : 8
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEMassociated_withimg Galactose C0016945
DISO_to_CHEMassociated_withimg Glucose C0017725
DISO_to_DISOmanifestation_ofimg Abnormal glucose oral tolerance test C1847425
DISO_to_DISOmanifestation_ofimg Caused by mutation in the intestinal sodium/glucose transporter gene (SLC5A1, 182380.0001). C1847427
DISO_to_DISOexpanded_form_ofimg Congenital glucose-galactose malabsorption C0268186
DISO_to_DISOmanifestation_ofimg Diarrhea, severe, chronic C1847423
DISO_to_DISOmanifestation_ofimg Failure to Thrive C0015544
DISO_to_DISOisaimg Glucose Intolerance C0271650
DISO_to_DISOmanifestation_ofimg Glucose breath hydrogen test shows malabsorption of glucose and galactose C1847426
DISO_to_DISOmanifestation_ofimg Glucosuria, mild, intermittent C1847424
DISO_to_DISOmanifestation_ofimg Hyperosmolar dehydration C1847428
DISO_to_DISOclinically_similarimg Lactose Intolerance C0022951
DISO_to_DISOmanifestation_ofimg Metabolic acidosis ICD10CM:E87.2 C3276544
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC5A16523solute carrier family 5 (sodium/glucose cotransporter), member 1
img GENERIF, Score=1000, Pubmed Id: 17903058, UMLKSK CUI: C0268186
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0268186Congenital glucose-galactose malabsorption0self