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Details
Link-It Detail - Disease - Hypokalemia
Debug Stats
  • ### Total Build Time: 482 ms 39.284 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 320 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 582 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= 232 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 563 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.526 KB
  • CONCEPT_RELATIONSHIPS gt=420 ms Completed: 420 ms rowSize= 14.127 KB
  • CONCEPT_GENES gt=30 ms Completed: 30 ms rowSize= 20.793 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypokalemia C0020621
Definition (1)
Abnormally low potassium concentration in the blood. It may result from potassium loss by renal secretion or by the gastrointestinal route, as by vomiting or diarrhea. It may be manifested clinically by neuromuscular disorders ranging from weakness to paralysis, by electrocardiographic abnormalities (depression of the T wave and elevation of the U wave), by renal disease, and by gastrointestinal disorders. (Dorland, 27th ed)
Semantic Types (2)
Finding (T033)
Disease or Syndrome (T047)
Parents (1)
img Water-Electrolyte Imbalance C0043065
Ancestral Roots
RootRoot Plus OneDepthParent
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Water-Electrolyte Imbalance C0043065
Relationships (152)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 94
diso_​to_​diso : 52
diso_​to_​phen : 4


Relationships:
none : 49
associated_​with : 1
classifies : 1
disease_​has_​finding : 3
isa : 6
mapped_​to : 9
may_​prevent : 37
may_​treat : 45
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 7
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO117img chemically induced C0007994
DISO_to_DISO106img Complication Aspects C1171258
DISO_to_DISO83img Complication Aspects C1171258
DISO_to_DISO68img chemically induced C0007994
DISO_to_ANAT60img In Blood C0005768
DISO_to_CHEM53img Potassium C0032821
DISO_to_DISO53img Hypertension C0020538
DISO_to_DISO39img Alkalosis C0002063
DISO_to_DISO36img Hypertension C0020538
DISO_to_PHEN34img genetic aspects C0017399
DISO_to_ANAT29img In Blood C0005768
DISO_to_CHEM26img Potassium C0032821
DISO_to_DISO26img Hyperkalemia C0020461
DISO_to_DISO26img Paralysis C0522224
DISO_to_DISO25img Paralysed C0522224
DISO_to_DISO24img Kidney Diseases C0022658
DISO_to_DISO22img ALDOSTERONISM C0020428
DISO_to_DISO22img Gitelman Syndrome C0268450
DISO_to_DISO22img RHABDOMYOLYSIS C0035410
DISO_to_DISO21img Arrhythmias, Cardiac C0003811
DISO_to_CHEM18img 720-724 DIURETICS C0012798
DISO_to_DISO18img DEFIC MAGNESIUM C0024473
DISO_to_CHEM17img Magnesium C0024467
DISO_to_DISO17img Hyperkalemia C0020461
DISO_to_DISO17img Hyponatremia C0020625
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A7115111solute carrier family 26 (anion exchanger), member 7
img GENERIF, Score=1000, Pubmed Id: 16524946, UMLKSK CUI: C0020621
HumanKCNE310008potassium voltage-gated channel, Isk-related family, member 3
img OMIM, Score=1000, UMLKSK CUI: C0020621
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanAIP9049aryl hydrocarbon receptor interacting protein
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanSLC12A36559solute carrier family 12 (sodium/chloride transporter), member 3
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanSLC2A26514solute carrier family 2 (facilitated glucose transporter), member 2
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanSCNN1G6340sodium channel, non-voltage-gated 1, gamma subunit
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanSCNN1B6338sodium channel, non-voltage-gated 1, beta subunit
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanSCN4A6329sodium channel, voltage-gated, type IV, alpha subunit
img OMIM, Score=1000, UMLKSK CUI: C0020621
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanPTEN5728phosphatase and tensin homolog
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanSMAD44089SMAD family member 4
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanKCNJ23759potassium inwardly-rectifying channel, subfamily J, member 2
img OMIM, Score=1000, UMLKSK CUI: C0020621
img OMIM, Score=761, UMLKSK CUI: C0020621
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanCYP11B11584cytochrome P450, family 11, subfamily B, polypeptide 1
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanCLCNKB1188chloride channel, voltage-sensitive Kb
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanCLCNKA1187chloride channel, voltage-sensitive Ka
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanCACNA1S779calcium channel, voltage-dependent, L type, alpha 1S subunit
img OMIM, Score=1000, UMLKSK CUI: C0020621
img OMIM, Score=1000, UMLKSK CUI: C0020621
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanBMPR1A657bone morphogenetic protein receptor, type IA
img OMIM, Score=1000, UMLKSK CUI: C0020621
HumanADRB2154adrenoceptor beta 2, surface
img GENERIF, Score=1000, Pubmed Id: 17292646, UMLKSK CUI: C0020621
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020621Hypokalemia0self