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Details
Link-It Detail - Disease - Learning Disorders
Debug Stats
  • ### Total Build Time: 261 ms 32.611 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 383 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=9 ms Completed: 9 ms rowSize= 1,016 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 546 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 6.713 KB
  • CONCEPT_RELATIONSHIPS gt=199 ms Completed: 199 ms rowSize= 13.643 KB
  • CONCEPT_GENES gt=26 ms Completed: 26 ms rowSize= 8.654 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Learning Disorders C0023186
Definition (1)
conditions characterized by a significant discrepancy between an individual's perceived level of intellect and their ability to acquire new language and other cognitive skills; may result from organic or psychological conditions.
Semantic Types (1)
Mental or Behavioral Dysfunction (T048)
Parents (2)
img Communication Disorders C0009460
img Mental Disorders Diagnosed in Childhood C0525040
Children (1)
img Dyslexia C0476254
Ancestral Roots
RootRoot Plus OneDepthParent
img Nervous System Diseases C0027765img Neurologic Manifestations C00278545img Communication Disorders C0009460
img Pathological Conditions, Signs and Symptoms C0039058img Signs and Symptoms C00370886img Communication Disorders C0009460
img Behavior and Behavior Mechanisms C0004928img Neurobehavioral Manifestations C05250414img Communication Disorders C0009460
img Mental Disorders C0004936img Mental Disorders Diagnosed in Childhood C05250404img Communication Disorders C0009460
img Mental Disorders C0004936img Mental Disorders Diagnosed in Childhood C05250403img Mental Disorders Diagnosed in Childhood C0525040
Relationships (120)

Relation Types:
diso_​to_​anat : 7
diso_​to_​chem : 5
diso_​to_​diso : 60
diso_​to_​phen : 2
diso_​to_​phys : 46


Relationships:
none : 110
isa : 2
mapped_​to : 1
permuted_​term_​of : 1
related_​to : 4
use : 2
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO161img Memory Disorders C0025261
DISO_to_DISO124img chemically induced C0007994
DISO_to_PHEN123img genetic aspects C0017399
DISO_to_DISO105img Complication Aspects C1171258
DISO_to_DISO96img Attention Deficit Disorder with Hyperactivity C1263846
DISO_to_DISO94img Memory Disorders C0025261
DISO_to_DISO84img Complication Aspects C1171258
DISO_to_DISO82img Cognition Disorders C0009241
DISO_to_PHEN79img genetic aspects C0017399
DISO_to_DISO69img Attention Deficit Disorder with Hyperactivity C1263846
DISO_to_DISO65img chemically induced C0007994
DISO_to_DISO59img Behavior Disorders, Child C0008066
DISO_to_DISO55img Intellectual Disability C0025362
DISO_to_ANAT51img Brain C0006104
DISO_to_ANAT51img Hippocampus (Brain) C0019564
DISO_to_DISO51img Developmental Disabilities C0008073
DISO_to_DISO46img Cognition Disorders C0009241
DISO_to_DISO45img Dyslexia C0476254
DISO_to_DISO44img Child Behavior Disorders C0008066
DISO_to_DISO42img Intellectual Disability C0025362
DISO_to_PHYS40img Cognition C0009240
DISO_to_ANAT38img Hippocampus C0019564
DISO_to_PHYS36img Learning, Verbal C0042531
DISO_to_DISO35img Dyslexia C0476254
DISO_to_DISO34img Epilepsy C0014544
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanDYX8406874dyslexia susceptibility 8
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanDYX1C1161582dyslexia susceptibility 1 candidate 1
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanDCDC251473doublecortin domain containing 2
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanDYX311192dyslexia susceptibility 3
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanSEMA4F10505sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4F
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanKIAA03199856KIAA0319
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanMRPL199801mitochondrial ribosomal protein L19
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanJMJD7-PLA2G4B8681
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanSLC6A36531solute carrier family 6 (neurotransmitter transporter), member 3
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanPLCB25330phospholipase C, beta 2
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanOTX15013orthodenticle homeobox 1
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanDRD41815dopamine receptor D4
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanDRD31814dopamine receptor D3
INFERRED, Score=800, UMLKSK CUI: C0023186
HumanDRD21813dopamine receptor D2
INFERRED, Score=800, UMLKSK CUI: C0023186
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0023186Learning Disorders0self