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Details
Link-It Detail - Disease - Polyuria
Debug Stats
  • ### Total Build Time: 189 ms 39.031 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 314 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 296 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= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=16 ms Completed: 16 ms rowSize= 998 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=18 ms Completed: 18 ms rowSize= 4.119 KB
  • CONCEPT_RELATIONSHIPS gt=108 ms Completed: 108 ms rowSize= 12.760 KB
  • CONCEPT_GENES gt=33 ms Completed: 33 ms rowSize= 19.225 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.143 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Polyuria C0032617
Definition (1)
Urination of a large volume of urine with an increase in urinary frequency, commonly seen in diabetes (DIABETES MELLITUS; DIABETES INSIPIDUS).
Semantic Types (1)
Sign or Symptom (T184)
Parents (2)
img Urination Disorders C0042035
img Urological Manifestations C0752303
Ancestral Roots
RootRoot Plus OneDepthParent
img Female Urogenital Diseases and Pregnancy Complications C1720765img Female Urogenital Diseases C17208875img Urination Disorders C0042035
img Male Urogenital Diseases C1720894img Urologic Diseases C00420754img Urination Disorders C0042035
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370884img Urological Manifestations C0752303
Relationships (31)

Relation Types:
diso_​to_​chem : 9
diso_​to_​diso : 15
diso_​to_​phen : 1
diso_​to_​phys : 6


Relationships:
none : 21
classifies : 2
isa : 1
mapped_​to : 3
may_​treat : 3
replaces : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO16img Complication Aspects C1171258
DISO_to_DISO14img Nocturia C0028734
DISO_to_DISO14img chemically induced C0007994
DISO_to_DISO13img chemically induced C0007994
DISO_to_DISO12img Complication Aspects C1171258
DISO_to_CHEM10img Agents, Anti-Diuretic C1563717
DISO_to_CHEM8img Deamino Arginine Vasopressin C0011701
DISO_to_DISO8img Disorder, Urination C0042035
DISO_to_DISO7img Hyponatremia C0020625
DISO_to_DISO7img Nocturnal Enuresis C0270327
DISO_to_CHEM6img Aquaporin 2 C0213238
DISO_to_DISO6img Central Diabetes Insipidus C0687720
DISO_to_DISO6img Diabetes Insipidus C0011848
DISO_to_CHEM5img Aquaporins C0599635
DISO_to_CHEM5img Arginine Vasopressin C0003779
DISO_to_CHEM5img Vasopressins C0042413
DISO_to_DISO5img Enuresis C0014394
DISO_to_PHEN5img genetic aspects C0017399
DISO_to_PHYS5img Circadian Rhythm C0008810
DISO_to_PHYS5img Diuresis C0012797
DISO_to_PHYS5img Thirst C0039971
DISO_to_CHEMmay_treatimg AMILORIDE C0002502
DISO_to_CHEMmay_treatimg AMILORIDE HCL 5MG ORAL TABLET C0687831
DISO_to_CHEMmay_treatimg AMILORIDE HYDROCHLORIDE C0546849
DISO_to_DISOisaimg Dipsogenic Diabetes Insipidus C0268813
Genes (22)

Species:
human : 22
SpeciesGeneGeneIdGene NameEvidence
HumanNPHP4261734nephronophthisis 4
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanFOXP350943forkhead box P3
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanNPHP327031nephronophthisis 3 (adolescent)
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanCLDN1610686claudin 16
img OMIM, Score=1000, UMLKSK CUI: C0032617
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanSH2B310019SH2B adaptor protein 3
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanHNF1A6927HNF1 homeobox A
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanSLC12A36559solute carrier family 12 (sodium/chloride transporter), member 3
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanSLC5A26524solute carrier family 5 (sodium/glucose cotransporter), member 2
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanOAS149382'-5'-oligoadenylate synthetase 1, 40/46kDa
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanNPHP14867nephronophthisis 1 (juvenile)
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanITPR33710inositol 1,4,5-trisphosphate receptor, type 3
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanHLA-DQB13119
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanCTNS1497cystinosin, lysosomal cystine transporter
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanCLCNKB1188chloride channel, voltage-sensitive Kb
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanCLCNKA1187chloride channel, voltage-sensitive Ka
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanCASR846calcium-sensing receptor
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanAVPR2554arginine vasopressin receptor 2
img OMIM, Score=1000, UMLKSK CUI: C0032617
HumanAQP2359aquaporin 2 (collecting duct)
img OMIM, Score=1000, UMLKSK CUI: C0032617
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0032617Polyuria0self