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 - Athetosis
Debug Stats
  • ### Total Build Time: 46 ms 19.370 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 316 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 591 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= 184 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 547 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.071 KB
  • CONCEPT_RELATIONSHIPS gt=22 ms Completed: 22 ms rowSize= 8.665 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 3.855 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.144 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Athetosis C0004158
Definition (1)
A dyskinesia characterized by an inability to maintain the fingers, toes, tongue, or other body parts in a stable position, resulting in continuous slow, sinusoidal, and flowing involuntary movements. This condition is frequently accompanied by CHOREA, where it is referred to as choreoathetosis. Athetosis may occur as a manifestation of BASAL GANGLIA DISEASES or DRUG TOXICITY. (From Adams et al., Principles of Neurology, 6th ed, p76)
Semantic Types (1)
Sign or Symptom (T184)
Parents (1)
img Dyskinesias C0013384
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Dyskinesias C0013384
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370885img Dyskinesias C0013384
img Nervous System Diseases C0027765img Neurologic Manifestations C00278544img Dyskinesias C0013384
Relationships (20)

Relation Types:
diso_​to_​chem : 1
diso_​to_​diso : 17
diso_​to_​phen : 2


Relationships:
none : 11
isa : 6
mapped_​to : 1
permuted_​term_​of : 1
used_​for : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO41img Chorea C0008489
DISO_to_DISO28img Chorea C0008489
DISO_to_DISO10img Complication Aspects C1171258
DISO_to_DISO10img Dystonia C0013421
DISO_to_DISO9img chemically induced C0007994
DISO_to_PHEN9img genetic aspects C0017399
DISO_to_DISO7img chemically induced C0007994
DISO_to_DISO6img Complication Aspects C1171258
DISO_to_DISO6img Dystonia C0013421
DISO_to_CHEM5img Anticonvulsants C0003286
DISO_to_PHEN5img genetic aspects C0017399
DISO_to_DISOused_forimg Abn involun movement NEC C0392702
DISO_to_DISOisaimg Athetoid paralysis C0234365
DISO_to_DISOpermuted_term_ofimg Athetosis C0004158
DISO_to_DISOisaimg Athetosis with rigidity C0270758
DISO_to_DISOisaimg Athetosis with spastic paraplegia C0270759
DISO_to_DISOmapped_toimg BRAIN-LUNG-THYROID SYNDROME C1970269
DISO_to_DISOisaimg Double athetosis C0270743
DISO_to_DISOisaimg O/E - athetosis C0437286
DISO_to_DISOisaimg Posthemiplegic athetosis C0270757
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanC10orf256652chromosome 10 open reading frame 2
img OMIM, Score=1000, UMLKSK CUI: C0004158
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
img OMIM, Score=1000, UMLKSK CUI: C0004158
HumanSMPD16609sphingomyelin phosphodiesterase 1, acid lysosomal
img OMIM, Score=1000, UMLKSK CUI: C0004158
HumanAUH549AU RNA binding protein/enoyl-CoA hydratase
img OMIM, Score=1000, UMLKSK CUI: C0004158
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0004158Athetosis0self