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Details
Link-It Detail - Disease - Epilepsy, Rolandic
Debug Stats
  • ### Total Build Time: 17 ms 11.258 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 501 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=4 ms Completed: 4 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.521 KB
  • CONCEPT_RELATIONSHIPS gt=5 ms Completed: 5 ms rowSize= 6.965 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Epilepsy, Rolandic C0376532
Definition (1)
An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and dysarthria. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Epilepsies, Partial C0014547
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076826img Epilepsies, Partial C0014547
Relationships (15)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 2
diso_​to_​diso : 8
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 13
mapped_​to : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO35img Complication Aspects C1171258
DISO_to_DISO22img Cognition Disorders C0009241
DISO_to_DISO21img Complication Aspects C1171258
DISO_to_PHEN13img genetic aspects C0017399
DISO_to_CHEM12img Anticonvulsants C0003286
DISO_to_DISO11img Cognition Disorders C0009241
DISO_to_CHEM10img Anticonvulsants C0003286
DISO_to_DISO8img Epilepsies, Partial C0014547
DISO_to_ANAT7img Brain C0006104
DISO_to_ANAT7img Cerebral Cortex C0007776
DISO_to_DISO7img Seizures C0036572
DISO_to_PHEN7img genetic aspects C0017399
DISO_to_PHYS7img Cognition C0009240
DISO_to_DISOmapped_toimg EPRPDC C1842531
DISO_to_DISOpermuted_term_ofimg Epilepsy, Rolandic C0376532
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0376532Epilepsy, Rolandic0self