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Details
Link-It Detail - Disease - Asperger Syndrome
Debug Stats
  • ### Total Build Time: 12 ms 17.952 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 337 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= 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= 574 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.540 KB
  • CONCEPT_RELATIONSHIPS gt=3 ms Completed: 3 ms rowSize= 12.317 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 1.511 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Asperger Syndrome C0236792
Definition (1)
neuropsychiatric disorder whose major manifestation is an inability to interact socially; other features include poor verbal and motor skills, singlemindedness, and social withdrawal.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Child Development Disorders, Pervasive C0008074
Ancestral Roots
RootRoot Plus OneDepthParent
img Mental Disorders C0004936img Mental Disorders Diagnosed in Childhood C05250404img Child Development Disorders, Pervasive C0008074
Relationships (31)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 15
diso_​to_​phen : 2
diso_​to_​phys : 12


Relationships:
none : 29
permuted_​term_​of : 1
related_​to : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO226img Autistic Disorder C0004352
DISO_to_DISO125img Autistic Disorder C0004352
DISO_to_DISO56img CHILD DEVELOPMENT DIS PERVASIVE C0008074
DISO_to_DISO52img Complication Aspects C1171258
DISO_to_DISO48img Complication Aspects C1171258
DISO_to_PHEN26img genetic aspects C0017399
DISO_to_PHEN22img genetic aspects C0017399
DISO_to_PHYS22img Pattern Recognition, Visual C0030709
DISO_to_PHYS22img Perception, Social C0037427
DISO_to_PHYS20img Attention C0004268
DISO_to_ANAT19img Brain C0006104
DISO_to_ANAT17img Brain C0006104
DISO_to_DISO17img Attention Deficit Disorder with Hyperactivity C1263846
DISO_to_DISO17img Cognition Disorders C0009241
DISO_to_DISO17img Language Development Disorders C0023014
DISO_to_DISO16img Cognition Disorders C0009241
DISO_to_PHYS16img Emotions C0013987
DISO_to_DISO15img Attention Deficit Disorder with Hyperactivity C1263846
DISO_to_DISO13img Expression, Facial C0015457
DISO_to_PHYS13img Intelligence C0021704
DISO_to_DISO12img CHILD DEVELOPMENT DIS PERVASIVE C0008074
DISO_to_PHYS12img Cognition C0009240
DISO_to_PHYS12img Concept, Self C0036594
DISO_to_PHYS12img Perception, Speech C0037826
DISO_to_PHYS11img Recognition C0524637
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanDISC127185disrupted in schizophrenia 1
img GENERIF, Score=1000, Pubmed Id: 17579608, UMLKSK CUI: C0236792
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0236792Asperger Syndrome0self