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 - Epilepsy, Benign Neonatal
Debug Stats
  • ### Total Build Time: 17 ms 22.077 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 402 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= 987 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.835 KB
  • CONCEPT_RELATIONSHIPS gt=10 ms Completed: 10 ms rowSize= 13.646 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 2.544 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Epilepsy, Benign Neonatal C0270851
Benign neonatal epilepsy
Definition (1)
An inherited or sporadic disorder characterized by epileptic seizures in the first four to six weeks of life. The seizures tend to subside after the fifteenth week of life.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Infant, Newborn, Diseases C0021290
img Epilepsy C0014544
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Infant, Newborn, Diseases C00212903img Infant, Newborn, Diseases C0021290
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Epilepsy C0014544
Relationships (43)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 28
diso_​to_​diso : 8
diso_​to_​phen : 2
diso_​to_​phys : 2


Relationships:
none : 8
is_​associated_​anatomic_​site_​of : 2
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 2
mapped_​to : 3
may_​treat : 26
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN45img genetic aspects C0017399
DISO_to_PHEN41img genetic aspects C0017399
DISO_to_CHEM22img KCNQ 002 POTASSIUM CHANNEL C0669669
DISO_to_PHYS13img Mutation C0026882
DISO_to_PHYS12img Mutation C0026882
DISO_to_DISO9img Complication Aspects C1171258
DISO_to_CHEM8img Potassium Channel C0032824
DISO_to_DISO8img Seizures C0036572
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Brain C0006104
DISO_to_ANATis_associated_anatomic_site_ofimg Central Nervous System C0927232
DISO_to_ANATis_associated_anatomic_site_ofimg Nervous System C0027763
DISO_to_CHEMmay_treatimg Monosodium Salt Phenobarbital C0282303
DISO_to_CHEMmay_treatimg PHENOBARBITAL 15 MG ORAL TABLET C0979441
DISO_to_CHEMmay_treatimg PHENOBARBITAL 15 MG/5 ML Oral (systemic) elixir C0979442
DISO_to_CHEMmay_treatimg PHENOBARBITAL 16 MG Oral (systemic) capsule C0689955
DISO_to_CHEMmay_treatimg PHENOBARBITAL 16 MG Oral (systemic) tablet C0689956
DISO_to_CHEMmay_treatimg PHENOBARBITAL 16.2 MG ORAL TABLET C0689957
DISO_to_CHEMmay_treatimg PHENOBARBITAL 18.5MG/5ML ELIXIR C0979445
DISO_to_CHEMmay_treatimg PHENOBARBITAL 20 MG ORAL ELIXIR C1878257
DISO_to_CHEMmay_treatimg PHENOBARBITAL 32MG CAP C0982831
DISO_to_CHEMmay_treatimg PHENOBARBITAL 32MG TAB C0979448
DISO_to_CHEMmay_treatimg PHENOBARBITAL 32MG TAB EC C0979449
DISO_to_CHEMmay_treatimg PHENOBARBITAL 60 MG ORAL TABLET C0689961
DISO_to_CHEMmay_treatimg PHENOBARBITAL 64.8 MG ORAL TABLET C0692501
DISO_to_CHEMmay_treatimg PHENOBARBITAL 65MG TAB C0979451
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanSCN2A6326sodium channel, voltage-gated, type II, alpha subunit
img OMIM, Score=909, UMLKSK CUI: C0270851
HumanKCNQ23785potassium voltage-gated channel, KQT-like subfamily, member 2
img GENERIF, Score=1000, Pubmed Id: 15596769, UMLKSK CUI: C0270851
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0270851Epilepsy, Benign Neonatal0self