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 - Cogan Syndrome
Debug Stats
  • ### Total Build Time: 27 ms 25.544 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 321 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 1.394 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 5.330 KB
  • CONCEPT_RELATIONSHIPS gt=4 ms Completed: 4 ms rowSize= 6.343 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 10.479 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Cogan Syndrome C0271270
Definition (1)
A condition consisting of inflammatory eye disease usually presenting as interstitial KERATITIS, vestibuloauditory dysfunction, and large- to medium-vessel vasculitis.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (3)
img Vestibulocochlear Nerve Diseases C0001163
img Vasculitis C0042384
img Eye Diseases C0015397
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Cranial Nerve Diseases C00102664img Vestibulocochlear Nerve Diseases C0001163
img Otorhinolaryngologic Diseases C0029896img Ear Diseases C00134475img Vestibulocochlear Nerve Diseases C0001163
img Cardiovascular Diseases C0007222img Vascular Diseases C00423734img Vasculitis C0042384
img Eye Diseases C0015397img Vascular Diseases C00423732img Eye Diseases C0015397
Relationships (14)

Relation Types:
diso_​to_​anat : 1
diso_​to_​chem : 3
diso_​to_​diso : 10


Relationships:
none : 11
mapped_​to : 2
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO22img Complication Aspects C1171258
DISO_to_DISO6img Hearing Loss, Sensorineural C0018784
DISO_to_ANAT2img In Blood C0005768
DISO_to_CHEM2img Antibodies, Monoclonal C0003250
DISO_to_CHEM2img GLUCOCORTICOIDS C0017710
DISO_to_CHEM2img Immunosuppressive Agents C0021081
DISO_to_DISO2img AUTOIMMUNE DIS C0004364
DISO_to_DISO2img CORONARY ARTERY OCCLUSION C0151814
DISO_to_DISO2img Hearing Loss C1384666
DISO_to_DISO2img Mitral Valve Insufficiency C0026266
DISO_to_DISO2img Uveitis C0042164
DISO_to_DISOmapped_toimg Anterior membrane corneal dystrophy C0521723
DISO_to_DISOmapped_toimg Apraxia, oculomotor, Cogan type C0543874
DISO_to_DISOpermuted_term_ofimg Cogan Syndrome C0271270
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanTMEM6791147transmembrane protein 67
img OMIM, Score=1000, UMLKSK CUI: C0271270
HumanCEP29080184centrosomal protein 290kDa
img OMIM, Score=1000, UMLKSK CUI: C0271270
HumanAPTX54840aprataxin
img GENERIF, Score=1000, Pubmed Id: 14534929, UMLKSK CUI: C0271270
img OMIM, Score=1000, UMLKSK CUI: C0271270
img OMIM, Score=1000, UMLKSK CUI: C0271270
img OMIM, Score=1000, UMLKSK CUI: C0271270
HumanAHI154806Abelson helper integration site 1
img OMIM, Score=1000, UMLKSK CUI: C0271270
HumanSETX23064senataxin
img OMIM, Score=1000, UMLKSK CUI: C0271270
HumanATXN26311ataxin 2
img OMIM, Score=1000, UMLKSK CUI: C0271270
HumanMAP2K25605mitogen-activated protein kinase kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0271270
HumanNPHP14867nephronophthisis 1 (juvenile)
img OMIM, Score=1000, UMLKSK CUI: C0271270
HumanGBA2629glucosidase, beta, acid
img OMIM, Score=1000, UMLKSK CUI: C0271270
HumanBRAF673v-raf murine sarcoma viral oncogene homolog B
img OMIM, Score=1000, UMLKSK CUI: C0271270
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0271270Cogan Syndrome0self