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 - Hypothalamic Diseases
Debug Stats
  • ### Total Build Time: 170 ms 36.146 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 340 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 430 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=26 ms Completed: 26 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= 550 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 1.832 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.516 KB
  • CONCEPT_RELATIONSHIPS gt=80 ms Completed: 80 ms rowSize= 12.396 KB
  • CONCEPT_GENES gt=46 ms Completed: 46 ms rowSize= 17.746 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.155 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypothalamic Diseases C0020655
Definition (1)
Neoplastic, inflammatory, infectious, and other diseases of the hypothalamus. Clinical manifestations include appetite disorders; AUTONOMIC NERVOUS SYSTEM DISEASES; SLEEP DISORDERS; behavioral symptoms related to dysfunction of the LIMBIC SYSTEM; and neuroendocrine disorders.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Brain Diseases C0006111
Children (4)
img Laurence-Moon Syndrome C0023138
img Hypothalamic Neoplasms C0020659
img Bardet-Biedl Syndrome C0752166
img Pituitary Diseases C0032002
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076824img Brain Diseases C0006111
Relationships (45)

Relation Types:
diso_​to_​anat : 7
diso_​to_​chem : 3
diso_​to_​diso : 33
diso_​to_​phen : 2


Relationships:
none : 33
isa : 9
mapped_​to : 2
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO103img Complication Aspects C1171258
DISO_to_DISO76img Hamartoma C0018552
DISO_to_DISO67img 755-756 HAMARTOMAS C0018552
DISO_to_DISO65img Complication Aspects C1171258
DISO_to_DISO30img Amenorrhea C0002453
DISO_to_DISO27img Epilepsies, Partial C0014547
DISO_to_DISO21img Epilepsies, Partial C0014547
DISO_to_PHEN20img genetic aspects C0017399
DISO_to_DISO18img Obesity C0028754
DISO_to_DISO18img Pituitary Diseases C0032002
DISO_to_ANAT17img In Blood C0005768
DISO_to_DISO16img Amenorrhea C0002453
DISO_to_ANAT15img Hypothalamic structure C0020663
DISO_to_DISO15img Precocious Puberty C0034013
DISO_to_ANAT14img Hypothalamic Pituitary Unit C0020662
DISO_to_DISO14img Epilepsy C0014544
DISO_to_DISO13img Obesity C0028754
DISO_to_DISO13img Pituitary Diseases C0032002
DISO_to_ANAT11img Hypothalamic structure C0020663
DISO_to_DISO11img Precocious Puberty C0034013
DISO_to_DISO10img Epilepsy C0014544
DISO_to_PHEN9img genetic aspects C0017399
DISO_to_DISO8img Autonomic Nervous System Diseases C1145628
DISO_to_ANAT7img Hypothalamic Pituitary Unit C0020662
DISO_to_ANAT7img In Blood C0005768
Genes (160)

Species:
human : 160
Page Size
Current 25
  Page 1 of 7
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMIR16-1406950
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanLIPI149998lipase, member I
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanBBS5129880Bardet-Biedl syndrome 5
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanTTC8123016tetratricopeptide repeat domain 8
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanHIST4H4121504histone cluster 4, H4
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanAPOA5116519apolipoprotein A-V
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanCSMD3114788CUB and Sushi multiple domains 3
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanTMEM6791147transmembrane protein 67
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanLHX489884LIM homeobox 4
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanTUBA1C84790tubulin, alpha 1c
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanARL684100ADP-ribosylation factor-like 6
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanINHBE83729inhibin, beta E
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanCEP29080184centrosomal protein 290kDa
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanBBS1079738Bardet-Biedl syndrome 10
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanCCDC28B79140coiled-coil domain containing 28B
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanPRX57716periaxin
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanAICDA57379activation-induced cytidine deaminase
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanBBS755212Bardet-Biedl syndrome 7
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanMKS154903Meckel syndrome, type 1
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanGHRL51738ghrelin/obestatin prepropeptide
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanIL23A51561interleukin 23, alpha subunit p19
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanANGPT451378angiopoietin 4
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanSOST50964sclerostin
INFERRED, Score=800, UMLKSK CUI: C0020655
HumanBBS927241Bardet-Biedl syndrome 9
INFERRED, Score=800, UMLKSK CUI: C0020655
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020655Hypothalamic Diseases0self