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Details
Link-It Detail - Disease - Hypokalemia
Debug Stats
  • ### Total Build Time: 185 ms 38.761 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 320 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 266 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=9 ms Completed: 9 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=161 ms Completed: 161 ms rowSize= 13.930 KB
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 20.775 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.146 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypokalemia C0020621
Definition (1)
A disorder characterized by laboratory test results that indicate a low concentration of potassium in the blood.
Semantic Types (2)
Disease or Syndrome (T047)
Finding (T033)
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 : 8
mapped_​to : 8
may_​prevent : 32
may_​treat : 50
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 Paralysed 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=761, UMLKSK CUI: C0020621
img OMIM, Score=1000, 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