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 - Perceptual Disorders
Debug Stats
  • ### Total Build Time: 35 ms 38.546 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 338 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 443 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= 201 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 566 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.229 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.135 KB
  • CONCEPT_RELATIONSHIPS gt=8 ms Completed: 8 ms rowSize= 12.149 KB
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 17.339 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Perceptual Disorders C0030975
Definition (1)
Cognitive disorders characterized by an impaired ability to perceive the nature of objects or concepts through use of the sense organs. These include spatial neglect syndromes, where an individual does not attend to visual, auditory, or sensory stimuli presented from one side of the body.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (1)
img Neurobehavioral Manifestations C0525041
Children (5)
img Hallucinations C0018524
img Agnosia C0001816
img Phantom Limb C0031315
img Illusions C0020903
img Auditory Perceptual Disorders C0004310
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Neurobehavioral Manifestations C0525041
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Neurobehavioral Manifestations C0525041
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250413img Neurobehavioral Manifestations C0525041
Relationships (52)

Relation Types:
diso_​to_​anat : 7
diso_​to_​diso : 22
diso_​to_​phys : 23


Relationships:
none : 51
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHYS218img Visual Perception C0042830
DISO_to_PHYS200img Space Perception C0037744
DISO_to_PHYS198img Visual Perception C0042830
DISO_to_PHYS181img Space Perception C0037744
DISO_to_PHYS149img Functional Laterality C1720777
DISO_to_PHYS142img Attention C0004268
DISO_to_PHYS119img Attention C0004268
DISO_to_DISO113img Cerebrovascular accident C0038454
DISO_to_PHYS98img Functional Laterality C1720777
DISO_to_PHYS90img Pattern Recognition, Visual C0030709
DISO_to_DISO88img Schizophrenia C0036341
DISO_to_DISO79img Complication Aspects C1171258
DISO_to_DISO79img Schizophrenia C0036341
DISO_to_DISO77img Cerebrovascular accident C0038454
DISO_to_DISO75img Cognition Disorders C0009241
DISO_to_PHYS74img Performance, Psychomotor C0033923
DISO_to_PHYS67img Performance, Psychomotor C0033923
DISO_to_ANAT66img Brain C0006104
DISO_to_DISO62img Cognition Disorders C0009241
DISO_to_DISO59img Complication Aspects C1171258
DISO_to_PHYS51img Orientation C0029266
DISO_to_PHYS48img Motion Perception C0026598
DISO_to_PHYS48img Pattern Recognition, Visual C0030709
DISO_to_PHYS45img Orientation C0029266
DISO_to_PHYS45img Perception, Time C0040226
Genes (55)

Species:
human : 55
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSCZD12619488schizophrenia 12
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanSCZD11404686Schizophrenia susceptibility locus, chromosome 10q-related
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanDAOA267012D-amino acid oxidase activator
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanDTNBP184062dystrobrevin binding protein 1
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanAPOL480832apolipoprotein L, 4
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanRTN4R65078reticulon 4 receptor
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanSCZD1063944schizophrenia disorder 10 (periodic catatonia)
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanJPH357338junctophilin 3
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanTREM254209triggering receptor expressed on myeloid cells 2
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanDISC127185disrupted in schizophrenia 1
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanDISC227184disrupted in schizophrenia 2 (non-protein coding)
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanUQCRQ27089ubiquinol-cytochrome c reductase, complex III subunit VII, 9.5kDa
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanAPOL223780apolipoprotein L, 2
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanATP13A223400ATPase type 13A2
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanHUWE110075HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanCLINT19685clathrin interactor 1
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanSCZD88806schizophrenia disorder 8
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanAPOL18542apolipoprotein L, 1
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanSCZD78401schizophrenia disorder 7
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanSCZD68400schizophrenia disorder 6
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanALDH5A17915aldehyde dehydrogenase 5 family, member A1
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanUQCRB7381ubiquinol-cytochrome c reductase binding protein
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanTYROBP7305TYRO protein tyrosine kinase binding protein
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanTBP6908TATA box binding protein
INFERRED, Score=800, UMLKSK CUI: C0030975
HumanSYN26854synapsin II
INFERRED, Score=800, UMLKSK CUI: C0030975
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0030975Perceptual Disorders0self