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Details
Link-It Detail - Disease - Alkalosis
Debug Stats
  • ### Total Build Time: 139 ms 23.703 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 316 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 229 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= 244 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=9 ms Completed: 9 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 560 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.519 KB
  • CONCEPT_RELATIONSHIPS gt=97 ms Completed: 97 ms rowSize= 13.058 KB
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 6.097 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.144 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Alkalosis C0002063
Definition (1)
A pathological condition that removes acid or adds base to the body fluids.
Semantic Types (2)
Pathologic Function (T046)
Disease or Syndrome (T047)
Parents (1)
img Acid-Base Imbalance C0001118
Children (1)
img Alkalosis, Respiratory C0002064
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Acid-Base Imbalance C0001118
Relationships (47)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 11
diso_​to_​diso : 30
diso_​to_​phen : 2
diso_​to_​phys : 2


Relationships:
none : 19
associated_​with : 1
classifies : 2
isa : 1
mapped_​to : 19
may_​treat : 5
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO39img Hypokalemia C0020621
DISO_to_DISO24img Acidosis C0001122
DISO_to_DISO24img chemically induced C0007994
DISO_to_DISO21img chemically induced C0007994
DISO_to_DISO17img Acidosis C0001122
DISO_to_PHEN17img genetic aspects C0017399
DISO_to_ANAT16img In Blood C0005768
DISO_to_DISO16img Complication Aspects C1171258
DISO_to_ANAT14img In Blood C0005768
DISO_to_CHEM12img Symporters C0598849
DISO_to_DISO12img Hypokalemia C0020621
DISO_to_PHYS12img Acid-Base Equilibrium C0001117
DISO_to_CHEM11img Magnesium C0024467
DISO_to_CHEM11img Sodium Bicarbonate C0074722
DISO_to_CHEM10img Calcium C0006675
DISO_to_DISO10img Complication Aspects C1171258
DISO_to_CHEM9img Carrier Protein C0007292
DISO_to_CHEM8img DRUG RECEPT C0034799
DISO_to_DISO8img Kidney Diseases C0022658
DISO_to_CHEMmay_treatimg ARGININE 10% INTRAVENOUS SOLUTION C0974540
DISO_to_CHEMmay_treatimg ARGININE 500 MG Oral (systemic) tablet C0692706
DISO_to_CHEMmay_treatimg ARGININE 700MG CAPSULE (HARD, SOFT, ETC.) C0978057
DISO_to_CHEMmay_treatimg Arginine C0003765
DISO_to_CHEMmay_treatimg Arginine hydrochloride C0301556
DISO_to_DISOclassifiesimg (Disorders of fluid, electrolyte and acid-base balance) or (electrolyte disorders) C0267994
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanTRPC47223transient receptor potential cation channel, subfamily C, member 4
img GENERIF, Score=861, Pubmed Id: 17074721, UMLKSK CUI: C0002063
HumanOTC5009ornithine carbamoyltransferase
INFERRED, Score=800, UMLKSK CUI: C0002063
HumanNOS34846nitric oxide synthase 3 (endothelial cell)
img GENERIF, Score=1000, Pubmed Id: 12060567, UMLKSK CUI: C0002063
HumanF2RL22151coagulation factor II (thrombin) receptor-like 2
img GENERIF, Score=1000, Pubmed Id: 15850610, UMLKSK CUI: C0002063
HumanCPS11373carbamoyl-phosphate synthase 1, mitochondrial
INFERRED, Score=800, UMLKSK CUI: C0002063
HumanASS1445argininosuccinate synthase 1
INFERRED, Score=800, UMLKSK CUI: C0002063
HumanASL435argininosuccinate lyase
INFERRED, Score=800, UMLKSK CUI: C0002063
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0002063Alkalosis0self