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 - Pituitary Diseases
Debug Stats
  • ### Total Build Time: 82 ms 40.142 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 420 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=9 ms Completed: 9 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 1,000 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 3.106 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.816 KB
  • CONCEPT_RELATIONSHIPS gt=40 ms Completed: 40 ms rowSize= 13.402 KB
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 17.740 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Pituitary Diseases C0032002
Definition (1)
Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Hypothalamic Diseases C0020655
img Endocrine System Diseases C0014130
Children (7)
img Empty Sella Syndrome C0014008
img Pituitary Neoplasms C0032019
img Pituitary Apoplexy C0032001
img Hypopituitarism C0020635
img Inappropriate ADH Syndrome C0021141
img Hyperpituitarism C0020506
img Diabetes Insipidus C0011848
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Hypothalamic Diseases C0020655
img Endocrine System Diseases C0014130img Central Nervous System Diseases C00076822img Endocrine System Diseases C0014130
Relationships (74)

Relation Types:
diso_​to_​anat : 12
diso_​to_​chem : 13
diso_​to_​diso : 47
diso_​to_​phen : 2


Relationships:
none : 33
associated_​with : 1
is_​associated_​anatomic_​site_​of : 2
isa : 23
location_​of : 1
mapped_​to : 1
may_​diagnose : 10
related_​to : 3
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO74img Complication Aspects C1171258
DISO_to_DISO54img Complication Aspects C1171258
DISO_to_ANAT53img Pituitary Gland C0032005
DISO_to_ANAT52img Pituitary Gland C0032005
DISO_to_DISO32img AUTOIMMUNE DIS C0004364
DISO_to_ANAT29img In Blood C0005768
DISO_to_DISO24img Pituitary Neoplasms C0032019
DISO_to_DISO22img Pituitary Neoplasms C0032019
DISO_to_PHEN20img genetic aspects C0017399
DISO_to_ANAT18img Pituitary Gland, Anterior C0032008
DISO_to_DISO18img AUTOIMMUNE DIS C0004364
DISO_to_DISO18img Hypothalamic Diseases C0020655
DISO_to_CHEM16img Human Growth Hormone C0169964
DISO_to_PHEN16img genetic aspects C0017399
DISO_to_ANAT15img Lymphocyte C0024264
DISO_to_CHEM15img Adrenocorticotropic Hormone C0001655
DISO_to_DISO15img Disease, Equine C0019940
DISO_to_DISO14img Adenoma C0001430
DISO_to_ANAT13img Pituitary Gland, Posterior C0032009
DISO_to_ANAT13img Sella Turcica C0036609
DISO_to_DISO13img Hypothalamic Diseases C0020655
DISO_to_ANAT12img In Blood C0005768
DISO_to_CHEM12img Human Growth Hormone C0169964
DISO_to_DISO12img Hypopituitarism C0020635
DISO_to_DISO12img Inflammation C0021368
Genes (157)

Species:
human : 157
Page Size
Current 25
  Page 1 of 7
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMIR16-1406950
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanLIPI149998lipase, member I
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanBBS5129880Bardet-Biedl syndrome 5
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanTTC8123016tetratricopeptide repeat domain 8
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanHIST4H4121504histone cluster 4, H4
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanAPOA5116519apolipoprotein A-V
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanCSMD3114788CUB and Sushi multiple domains 3
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanTMEM6791147transmembrane protein 67
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanLHX489884LIM homeobox 4
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanTUBA1C84790tubulin, alpha 1c
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanARL684100ADP-ribosylation factor-like 6
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanINHBE83729inhibin, beta E
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanCEP29080184centrosomal protein 290kDa
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanBBS1079738Bardet-Biedl syndrome 10
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanPRX57716periaxin
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanAICDA57379activation-induced cytidine deaminase
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanBBS755212Bardet-Biedl syndrome 7
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanMKS154903Meckel syndrome, type 1
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanGHRL51738ghrelin/obestatin prepropeptide
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanIL23A51561interleukin 23, alpha subunit p19
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanANGPT451378angiopoietin 4
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanSOST50964sclerostin
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanBBS927241Bardet-Biedl syndrome 9
INFERRED, Score=800, UMLKSK CUI: C0032002
HumanRHBDD325807rhomboid domain containing 3
INFERRED, Score=800, UMLKSK CUI: C0032002
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0032002Pituitary Diseases0self