Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Disease - 4-71 CONGENITAL ANOMALIES OF THE KIDNEYS
Debug Stats
  • ### Total Build Time: 148 ms 35.321 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=91 ms Completed: 91 ms rowSize= 12.167 KB
  • CONCEPT_GENES gt=37 ms Completed: 37 ms rowSize= 21.541 KB
  • CONCEPT_XREFS gt=15 ms Completed: 15 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
4-71 CONGENITAL ANOMALIES OF THE KIDNEYS C0266292
Relationships (31)

Relation Types:
diso_​to_​anat : 1
diso_​to_​diso : 30


Relationships:
associated_​with : 1
isa : 29
location_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATlocation_ofimg Kidney C0022646
DISO_to_DISOisaimg Accessory kidney C0266298
DISO_to_DISOisaimg Allanson Pantzar McLeod syndrome C0266313
DISO_to_DISOisaimg Bifid kidney C0345331
DISO_to_DISOisaimg Branchio-Oto-Renal Syndrome C0265234
DISO_to_DISOassociated_withimg Congenital Abnormalities C0000768
DISO_to_DISOisaimg Congenital Nephrotic Syndrome C0268713
DISO_to_DISOisaimg Congenital abnormal shape of kidney C0685822
DISO_to_DISOisaimg Congenital absence of kidney C0542519
DISO_to_DISOisaimg Congenital anomaly of renal blood vessel C2316098
DISO_to_DISOisaimg Congenital anomaly of renal pelvis C0266314
DISO_to_DISOisaimg Congenital atrophy of kidney C0266293
DISO_to_DISOisaimg Congenital calculus of kidney C0266300
DISO_to_DISOisaimg Congenital calyceal diverticulum C0345332
DISO_to_DISOisaimg Congenital cystic kidney disease C0311245
DISO_to_DISOisaimg Congenital displaced kidney C0266301
DISO_to_DISOisaimg Congenital enlarged kidney C0266306
DISO_to_DISOisaimg Congenital fusion of kidneys C0266305
DISO_to_DISOisaimg Congenital hydrocalicosis C0431704
DISO_to_DISOisaimg Congenital hypoplasia of kidney C0266295
DISO_to_DISOisaimg Congenital nephritis C0349480
DISO_to_DISOisaimg Congenital obstructive defect of renal pelvis C0431723
DISO_to_DISOisaimg Congenital renal failure C0410932
DISO_to_DISOisaimg Congenital uraemia C0343305
DISO_to_DISOisaimg Discoid kidney C0266308
Genes (24)

Species:
human : 24
SpeciesGeneGeneIdGene NameEvidence
HumanBBS12166379Bardet-Biedl syndrome 12
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanBBS5129880Bardet-Biedl syndrome 5
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanTTC8123016tetratricopeptide repeat domain 8
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanTMEM6791147transmembrane protein 67
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanARL684100ADP-ribosylation factor-like 6
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanCEP29080184centrosomal protein 290kDa
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanBBS1079738Bardet-Biedl syndrome 10
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanSALL457167sal-like 4 (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0266292
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanBBS755212Bardet-Biedl syndrome 7
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanMKS154903Meckel syndrome, type 1
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanBBS927241Bardet-Biedl syndrome 9
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanTRIM3222954tripartite motif containing 32
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanCLINT19685clathrin interactor 1
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanRECQL49401RecQ protein-like 4
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanMKKS8195McKusick-Kaufman syndrome
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanPAX87849paired box 8
img GENERIF, Score=844, Pubmed Id: 15355349, UMLKSK CUI: C0266292
HumanALMS17840Alstrom syndrome 1
img OMIM, Score=858, UMLKSK CUI: C0266292
HumanHNF1B6928HNF1 homeobox B
img GENERIF, Score=844, Pubmed Id: 15355349, UMLKSK CUI: C0266292
HumanGATA32625GATA binding protein 3
img GENERIF, Score=734, Pubmed Id: 16509533, UMLKSK CUI: C0266292
HumanFANCA2175Fanconi anemia, complementation group A
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanEYA12138eyes absent homolog 1 (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanBBS4585Bardet-Biedl syndrome 4
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanBBS2583Bardet-Biedl syndrome 2
img OMIM, Score=1000, UMLKSK CUI: C0266292
HumanBBS1582Bardet-Biedl syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0266292
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C02662924-71 CONGENITAL ANOMALIES OF THE KIDNEYS0self