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Details
Link-It Detail - Disease - Nephrosis
Debug Stats
  • ### Total Build Time: 32 ms 38.205 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 316 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 448 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=3 ms Completed: 3 ms rowSize= 991 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.812 KB
  • CONCEPT_RELATIONSHIPS gt=5 ms Completed: 5 ms rowSize= 12.725 KB
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 19.062 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.144 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Nephrosis C0027720
Definition (1)
Pathological processes of the KIDNEY without inflammatory or neoplastic components. Nephrosis may be a primary disorder or secondary complication of other diseases. It is characterized by the NEPHROTIC SYNDROME indicating the presence of PROTEINURIA and HYPOALBUMINEMIA with accompanying EDEMA.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Kidney Diseases C0022658
Children (2)
img Nephrotic Syndrome C0027726
img Nephrosis, Lipoid C0027721
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 (28)

Relation Types:
diso_​to_​anat : 7
diso_​to_​chem : 7
diso_​to_​diso : 13
diso_​to_​phen : 1


Relationships:
none : 21
associated_​with : 1
location_​of : 1
mapped_​to : 4
permuted_​term_​of : 1
Page Size
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Prior Page
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO51img chemically induced C0007994
DISO_to_DISO37img chemically induced C0007994
DISO_to_DISO16img Proteinuria C0033687
DISO_to_ANAT14img Kidney C0022646
DISO_to_ANAT13img Epithelial Cells, Glomerular Visceral C1328818
DISO_to_ANAT12img Kidney Glomerulus C0022663
DISO_to_DISO11img Complication Aspects C1171258
DISO_to_ANAT10img Kidney Glomerulus C0022663
DISO_to_CHEM10img 3' Amino 3' deoxy N,N dimethyladenosine C0034146
DISO_to_CHEM9img 3' Amino 3' deoxy N,N dimethyladenosine C0034146
DISO_to_CHEM9img Membrane Associated Proteins C0025252
DISO_to_CHEM8img Membrane Associated Proteins C0025252
DISO_to_DISO8img Complication Aspects C1171258
DISO_to_ANAT7img In Blood C0005768
DISO_to_ANAT6img In Blood C0005768
DISO_to_CHEM6img Angiotensin-Converting Enzyme Inhibitors C0003015
DISO_to_DISO6img Proteinuria C0033687
DISO_to_CHEM5img Chinese Drugs, Plant C0013229
DISO_to_CHEM5img Cyclosporine C0010592
DISO_to_DISO5img Focal glomerulosclerosis C0017668
DISO_to_PHEN5img genetic aspects C0017399
DISO_to_ANATlocation_ofimg Kidney C0022646
DISO_to_DISOmapped_toimg Barakat syndrome C1840333
DISO_to_DISOassociated_withimg Disease C0012634
DISO_to_DISOmapped_toimg GALLOWAY SYNDROME C0795949
Genes (55)

Species:
human : 55
Page Size
Current 25
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Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMUC1694025mucin 16, cell surface associated
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanLMNB284823lamin B2
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanADCK356997aarF domain containing kinase 3
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanAPTX54840aprataxin
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanPLCE151196phospholipase C, epsilon 1
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanHSPC15929094
img GENERIF, Score=694, Pubmed Id: 18219197, UMLKSK CUI: C0027720
HumanCOQ227235coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanPDSS123590prenyl (decaprenyl) diphosphate synthase, subunit 1
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanTNFSF108743tumor necrosis factor (ligand) superfamily, member 10
img GENERIF, Score=694, Pubmed Id: 15671071, UMLKSK CUI: C0027720
HumanNPHS27827nephrosis 2, idiopathic, steroid-resistant (podocin)
img GAD, Score=1000, Pubmed Id: 15769810, UMLKSK CUI: C0027720
HumanWT17490Wilms tumor 1
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanTGFB17040transforming growth factor, beta 1
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanTFPI7035tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanSTAT66778signal transducer and activator of transcription 6, interleukin-4 induced
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanRELA5970v-rel avian reticuloendotheliosis viral oncogene homolog A
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanPMM25373phosphomannomutase 2
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanNPPC4880natriuretic peptide C
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanNPHS14868nephrosis 1, congenital, Finnish type (nephrin)
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanMEFV4210Mediterranean fever
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanMAF4094v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
INFERRED, Score=800, UMLKSK CUI: C0027720
HumanLYZ4069lysozyme
INFERRED, Score=800, UMLKSK CUI: C0027720
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0027720Nephrosis0self