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 - Goiter
Debug Stats
  • ### Total Build Time: 212 ms 42.213 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 310 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 326 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= 552 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.234 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.505 KB
  • CONCEPT_RELATIONSHIPS gt=173 ms Completed: 173 ms rowSize= 14.528 KB
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 21.434 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.141 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Goiter C0018021
Definition (1)
Enlargement of the thyroid gland usually caused by lack of iodine in the diet, hyperthyroidism, or thyroid nodules. Symptoms include difficulty in breathing and swallowing.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Thyroid Diseases C0040128
Children (5)
img Lingual Goiter C0271760
img Goiter, Nodular C0018023
img Goiter, Endemic C0018022
img Goiter, Substernal C0018024
img Graves Disease C0018213
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C0014130img Thyroid Diseases C00401283img Thyroid Diseases C0040128
Relationships (149)

Relation Types:
diso_​to_​anat : 9
diso_​to_​chem : 89
diso_​to_​diso : 49
diso_​to_​phen : 2


Relationships:
none : 33
associated_​with : 1
classifies : 2
is_​associated_​anatomic_​site_​of : 2
is_​normal_​tissue_​origin_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 11
location_​of : 1
mapped_​to : 16
may_​treat : 81
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM106img Iodine C0021968
DISO_to_CHEM74img Iodine C0021968
DISO_to_ANAT72img Thyroid Gland C0040132
DISO_to_DISO69img Complication Aspects C1171258
DISO_to_DISO62img Complication Aspects C1171258
DISO_to_ANAT61img Thyroid Gland C0040132
DISO_to_DISO47img Thyroid Neoplasm C0040136
DISO_to_DISO46img HYPOTHYROIDISM C0020676
DISO_to_PHEN45img genetic aspects C0017399
DISO_to_DISO42img Thyroid Neoplasm C0040136
DISO_to_PHEN40img genetic aspects C0017399
DISO_to_ANAT26img In Blood C0005768
DISO_to_CHEM26img Sodium Chloride, Dietary C0206136
DISO_to_DISO25img Congenital Hypothyroidism C0010308
DISO_to_DISO24img HYPOTHYROIDISM C0020676
DISO_to_ANAT21img In Blood C0005768
DISO_to_DISO21img DISORDER FETAL C0015929
DISO_to_CHEM19img Sodium Chloride, Dietary C0206136
DISO_to_DISO18img chemically induced C0007994
DISO_to_CHEM17img Thyroxine C0040165
DISO_to_DISO16img Carcinoma, Papillary C0007133
DISO_to_CHEM15img Membrane Transport Proteins C0596902
DISO_to_CHEM14img Iodine Radioisotopes C0021970
DISO_to_DISO14img Graves Disease C0018213
DISO_to_DISO14img HYPERTHYROIDISM C0020550
Genes (103)

Species:
human : 103
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanIYD389434iodotyrosine deiodinase
img GENERIF, Score=1000, Pubmed Id: 18434651, UMLKSK CUI: C0018021
img OMIM, Score=1000, UMLKSK CUI: C0018021
HumanGRDX117189Graves disease, susceptibility to, X-linked
img OMIM, Score=1000, UMLKSK CUI: C0018021
HumanSCGB3A2117156secretoglobin, family 3A, member 2
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanFCRL3115352Fc receptor-like 3
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanIFIH164135interferon induced with helicase C domain 1
img OMIM, Score=1000, UMLKSK CUI: C0018021
HumanUACA55075uveal autoantigen with coiled-coil domains and ankyrin repeats
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanGRD250976Graves disease, susceptibility to, 2
img OMIM, Score=1000, UMLKSK CUI: C0018021
HumanCD27429126CD274 molecule
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanPTPN2226191protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanPRDX525824peroxiredoxin 5
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanCXCR610663chemokine (C-X-C motif) receptor 6
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanPAX87849paired box 8
img OMIM, Score=1000, UMLKSK CUI: C0018021
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanTNFRSF47293tumor necrosis factor receptor superfamily, member 4
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanTSHR7253thyroid stimulating hormone receptor
img OMIM, Score=1000, UMLKSK CUI: C0018021
HumanTPO7173thyroid peroxidase
img OMIM, Score=1000, UMLKSK CUI: C0018021
HumanTNFRSF1B7133tumor necrosis factor receptor superfamily, member 1B
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanTHY17070Thy-1 cell surface antigen
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanTHRB7068thyroid hormone receptor, beta
img OMIM, Score=1000, UMLKSK CUI: C0018021
HumanTGFB17040transforming growth factor, beta 1
INFERRED, Score=800, UMLKSK CUI: C0018021
HumanTG7038thyroglobulin
img GENERIF, Score=1000, Pubmed Id: 17911408, UMLKSK CUI: C0018021
HumanTEK7010TEK tyrosine kinase, endothelial
img GENERIF, Score=694, Pubmed Id: 15817662, UMLKSK CUI: C0018021
HumanTAP26891transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)
INFERRED, Score=800, UMLKSK CUI: C0018021
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0018021Goiter0self