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Details
Link-It Detail - Disease - Renal Insufficiency
Debug Stats
  • ### Total Build Time: 164 ms 37.902 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 498 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=1 ms Completed: 1 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 551 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 566 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.812 KB
  • CONCEPT_RELATIONSHIPS gt=126 ms Completed: 126 ms rowSize= 13.302 KB
  • CONCEPT_GENES gt=21 ms Completed: 21 ms rowSize= 18.520 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Renal Insufficiency C1565489
Definition (1)
Conditions in which the KIDNEYS perform below the normal level in the ability to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. Renal insufficiency can be classified by the degree of kidney damage (as measured by the level of PROTEINURIA) and reduction in GLOMERULAR FILTRATION RATE.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Kidney Diseases C0022658
Children (1)
img Renal Insufficiency, Chronic C0403447
Ancestral Roots
RootRoot Plus OneDepthParent
img Female Urogenital Diseases and Pregnancy Complications C1720765img Female Urogenital Diseases C17208875img Kidney Diseases C0022658
img Male Urogenital Diseases C1720894img Urologic Diseases C00420754img Kidney Diseases C0022658
Relationships (168)

Relation Types:
diso_​to_​anat : 10
diso_​to_​chem : 64
diso_​to_​diso : 86
diso_​to_​phen : 2
diso_​to_​phys : 6


Relationships:
none : 162
mapped_​to : 5
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 7
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO578img Complication Aspects C1171258
DISO_to_DISO371img Complication Aspects C1171258
DISO_to_DISO295img chemically induced C0007994
DISO_to_ANAT241img In Blood C0005768
DISO_to_DISO197img chemically induced C0007994
DISO_to_ANAT184img Kidney C0022646
DISO_to_ANAT170img In Blood C0005768
DISO_to_DISO125img Heart Failure C0018801
DISO_to_CHEM120img Contrast Media C0009924
DISO_to_ANAT106img Kidney C0022646
DISO_to_PHEN72img genetic aspects C0017399
DISO_to_DISO68img Hypertension C0020538
DISO_to_CHEM63img Contrast Media C0009924
DISO_to_DISO60img Multiple Myeloma C0026764
DISO_to_CHEM59img Creatinine C0010294
DISO_to_DISO59img Heart Failure C0018801
DISO_to_CHEM54img Gadolinium C0016911
DISO_to_DISO53img Dermatologic disorders C0037274
DISO_to_DISO49img Cardiovascular Diseases C0007222
DISO_to_DISO46img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_DISO45img Kidney Diseases C0022658
DISO_to_DISO44img Hypertension C0020538
DISO_to_DISO43img Cardiovascular Diseases C0007222
DISO_to_DISO40img COMPL POSTOP C0032787
DISO_to_CHEM39img Antineoplastic Agents C0003392
Genes (150)

Species:
human : 150
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanNPHP4261734nephronophthisis 4
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanSLC22A12116085solute carrier family 22 (organic anion/urate transporter), member 12
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanNLRP3114548NLR family, pyrin domain containing 3
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanHPS489781Hermansky-Pudlak syndrome 4
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanDTNBP184062dystrobrevin binding protein 1
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanCEP29080184centrosomal protein 290kDa
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanHPS679803Hermansky-Pudlak syndrome 6
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanXYLT264132xylosyltransferase II
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanXYLT164131xylosyltransferase I
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanRETN56729resistin
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanAHI154806Abelson helper integration site 1
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanINVS27130inversin
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanNPHP327031nephronophthisis 3 (adolescent)
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanHPS511234Hermansky-Pudlak syndrome 5
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanADAMTS1311093ADAM metallopeptidase with thrombospondin type 1 motif, 13
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanUTS210911urotensin 2
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanCLDN1610686claudin 16
img GENERIF, Score=1000, Pubmed Id: 16924549, UMLKSK CUI: C1565489
HumanHYOU110525hypoxia up-regulated 1
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanMERTK10461c-mer proto-oncogene tyrosine kinase
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanNAMPT10135nicotinamide phosphoribosyltransferase
INFERRED, Score=800, UMLKSK CUI: C1565489
HumanIQCB19657IQ motif containing B1
INFERRED, Score=800, UMLKSK CUI: C1565489
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1565489Renal Insufficiency0self